Lead Opinion
Opinion for the court by Judge NEWMAN except for Part I.E (on-sale issue) and Part VI.C (attempt to monopolize). Judge BRYSON does not join Parts I.A-D of Judge NEWMAN’S opinion. The district court’s judgment concerning the on-sale bar is affirmed in separate opinions by Chief Judge MAYER and Judge BRYSON. The district court’s judgment concerning the attempt to monopolize issue is reversed-in-part by Judge NEWMAN’S opinion (Parts VI.A-B), which Chief Judge MAYER and Judge BRYSON join, and affirmed-in-part by Judge BRYSON’S opinion (Part II), which Chief Judge MAYER joins. Judge NEWMAN dissents with respect to the on-sale bar and attempt to monopolize issues.
In suit are United States Patent No. 4,944,308 issued July 31, 1990 (the ’308 patent) and United States Reissue Patent No. RE 34,056 issued September 8,1992 (the ’056 patent), both entitled “Tissue Sampling Device.” These patents originated with the work of Dr. Per Gunner Lindgren, a physician in Sweden, and are now owned by appellant C.R. Bard, Inc.
The patented inventions are devices for taking samples of body tissue for biopsy purposes, wherein a biopsy needle firing device or “gun” mechanically injects a biopsy needle assembly into the core body tissue. These devices are. described as improving the speed, accuracy, ease, and patient comfort of tissue sampling, compared with manually inserted biopsy needles. They are said to be particularly advantageous for sampling small or movable lesions and fibrous or firm tissues, because the rapidly and firmly fired needles can penetrate even fibrotic lesions before the lesions can slip aside. The patented guns and needles have achieved commercial success.
Bard sued M3 Systems in August 1993 in the United States District Court for the Northern District of Illinois,
The district court denied all post-trial motions. This appeal followed. This court affirms the judgment of invalidity of the ’056 patent and vacates the judgment of nonin-fringement of the ’056 patent. The judgment of invalidity of the ’308 patent is reversed and the judgment of noninfringement is affirmed. The judgments of misuse and fraud are reversed. The judgment of antitrust violation on the ground of attempt to monopolize is affirmed, but the antitrust damages award is vacated, for redetermination upon remand.
THE PATENTED INVENTIONS
The First Generation Device — The PCT Patent Application
In 1981 Dr. Lindgren, working in Sweden with Jan Allard, an engineer, designed and
This procedure required the physician to use both hands to manipulate the needles, while a second physician would hold and manipulate the ultrasound equipment that is usually required to view the interior of the body and direct insertion of the needles. Dr. Lindgren sought to mechanize this procedure in order to improve the speed and accuracy of insertion, to reduce human error, and to permit a physician to perform the biopsy without assistance by providing a sampling device that can be operated with one hand while the other hand holds the ultrasound apparatus.
The first generation gun is a box-like structure fitted with two spring-loaded drivers associated with slots that are configured to hold the cannula and stylet of the Tru-Cut needle assembly. To use this gun the physician must first “cock” each of the spring-loaded drivers. This cocking action, as it was often called at trial, is referred to as pre-tensioning or energizing in the patent documents. Cocking is performed by hand or with a specially designed tool described as a miniature crowbar. After the drivers are cocked, the stylet and cannula are placed in the appropriate slots and the gun housing is closed. The gun is then aimed at the target tissue and a trigger mechanism releases the stylet and cannula in rapid sequence. The needles are then manually retrieved.
Dr. Lindgren and Mr. Allard filed a patent application on the first generation gun under the Patent Cooperation Treaty (PCT). The invention was assigned to Radiplast AB, a small Swedish company associated with Dr. Lindgren. The PCT application was filed on March 31, 1982 and was published on October 13, 1983. It is prior art to the United States patents in suit.
The Second Generation — The ’056 Reissue Patent
Starting in 1984, Dr. Lindgren undertook to improve the gun so that it would not be necessary for the physician to cock the two drivers manually before installing the biopsy needles, a step described as awkward and inefficient. In 1985 Dr. Lindgren, working with Dan Akerfeldt, an engineer, designed a mechanism whereby the drivers are cocked by external action after the needles are placed in the gun and the housing is closed. In this mechanism rods are attached to each of the spring-loaded drivers, extend out the back of the gun, and culminate in a ring or handle. By pulling the ring or handle the operator simultaneously cocks both drivers, moving, the needles rearward. A trigger mechanism then fires the stylet and cannula, in rapid sequence, into the tissue to be sampled.
The Tru-Cut needles were not usable with the second generation gun, for their structure was such that they could not be moved rearward as well as propelled forward. New needles were designed with a modified hub and flange structure and a slit in the stylet flange to facilitate placement in the gun. Corresponding structural changes were made to the gun to accommodate the changes in the needles. Radiplast, as assignee, filed a patent application in Sweden on February 19, 1986. The United States application was filed on July 30, 1986, naming Dr. Lindgren as the inventor. Corresponding United States Patent No. 4,699,154 (the ’154 patent) was issued on October 13,1987, with claims to the combination of the second generation gun and the new needle assémbly. The ’154 patent did not claim the needle assembly alone.
The Third Generation Gun—The ’308 Patent
Dan Ákerfeldt continued to work on improving these devices. He sought to make the gun easier to use, especially by inexperienced physicians. Because pulling the cocking ring required significant manual force to overcome the simultaneous resistance of both driver springs, he designed an external integrated cocking mechanism that energized the two springs sequentially, thereby requiring less force than did the simultaneous cocking mechanism of the second generation gun. The third generation gun also provided for separate rearward movement of the needles after the biopsy sample was taken, thereby facilitating removal of the tissue from the stylet. Radiplast applied for a United States patent on the third generation gun on November 14, 1988, naming Dan Ákerfeldt as inventor. The patent issued in 1990 and is the ’308 patent in suit.
I
VALIDITY OF THE ’056 REISSUE PATENT
Bard charged M3 Systems with infringement of claims 9-12 and 21-23 of the ’056 patent. M3 had the burden of establishing invalidity by clear and convincing evidence at trial. Carella v. Starlight Archery,
When a claim or defense can not be maintained or defeated without a favorable finding on a material issue, and there is not substantial evidence supporting that finding, the verdict can not stand and the court must render judgment as a matter of law. See Fed.R.Civ.P. 50; Anderson v. Liberty Lobby, Inc.,
We apply these principles to each of the grounds on which the jury rendered verdicts of invalidity of the asserted ’056 claims. We direct our discussion of validity primarily to claim 21, for the claim is representative and M3 Systems’ expert witnesses admitted infringement of claim 21 by M3’s original ACN needles:
21. A biopsy needle for use with a tissue sampling device having a housing with a forward end, a first slide mounted for longitudinal motion within said housing, and a second slide mounted for longitudi*1349 nal motion within said housing, said biopsy-needle comprising:
a hollow first needle having proximal and distal ends;
a second needle extending through said hollow first needle and freely slidable ther-ewithin, said second needle having proximal and distal ends;
a first head mounted to said proximal end of.said hollow first needle, said first head including first flange means associated therewith for coupling said hollow first needle to said first slide for longitudinal motion both toward and away from said forward end of said housing; and
a second head mounted to said proximal end of said second needle, said second head including second flange means associated therewith for coupling said second needle to said second slide for longitudinal motion both toward and away from said forward end of said housing.
A, Anticipation
To meet the requirements of patenta-bility a device must be new; that is, it must not have been previously known. Section 102(a) requires that the subject matter was not published anywhere, or known or used by others in the United States, before its invention by the patentee.
When the defense of lack of novelty is based on a printed publication that is asserted to describe the same invention, a finding of anticipation requires that the publication describe all of the elements of the claims, arranged as in the patented device. Shearing v. Iolab Corp.,
The district court declined to construe all of the claim terms that were placed in dispute, instructing the jury that “words in a claim are to be given their ordinary and accustomed meaning, unless it appears that the inventor intended to use them differently.... You may use the specification to interpret what the patentee meant by a word or phrase in a claim.” The record shows that the court defined some terms and the parties explained their views to the jury. This procedure was not incorrect at the time this case was tried-for as the court observed, the question of the relative roles of judge and jury was then before the Supreme Court- and does not of itself warrant a new trial. On appellate review, however, we apply the principles of Cybor Corp. v. FAS Techs., Inc.,
1. The Term “Freely Slidable”
M3 Systems contends that the claim term “freely slidable” does not distinguish
a second needle extending through said hollow first needle and freely slidable ther-ewithal, ...
Bard argues that the court should have construed “freely slidable” for the jury, and that correctly construed this term means that the needle slides freely in either direction. M3 responds that Bard improperly seeks to insert the limitation “totally” into the definition of “freely slidable” and that, correctly construed, “freely slidable” requires only sliding freely in the forward direction. M3 states that since the Tru-Cut is freely slidable in the forward direction, the claim reads on the prior art and is invalid for anticipation.
M3 Systems’ proposed claim construction is not correct, and could not have reasonably been adopted. The specification leaves no uncertainty that the ’056 needles are freely slidable in both directions, for that is a purpose of the new ’056 needle structure. M3’s proposed interpretation is unsupported by, and indeed is contrary to, the specification. See Slimfold Mfg. Co. v. Kinkead Indus., Inc.,
2. The “Housing”
M3 Systems argues that the preamble of the ’056 claims refers only to the “housing” of the tissue sampling device, and that the lack of any preamble reference to an external automatic cocking mechanism invalidates the claims by anticipation because they fail to distinguish the gun of the preamble from the prior art first generation gun.
M3 Systems has incorrectly construed the claim preamble. A preamble may serve a variety of purposes, depending on its content. It may limit the scope of the claim, for example when patentability depends on limitations stated in the preamble, as in In re Stencel,
In the case at bar, the preamble of claim 21 recites the portion and structure of the gun housing into which the needles fit, and provides reference points in the gun that aid in defining the needles as set forth in the body of the claim. M3 Systems is incorrect in stating that the preamble must contain details of the integrated mechanical cocking structure, for the gun structure is not part of the separate claims to the needles. The question of anticipation of the ’056 claims relates to the needles, not the gun. To the extent that the jury verdicts of anticipation may have been based on M3’s incorrect construction of the preamble, they can not be sustained. On the correct construction of the preamble, it contributes no basis of invalidity on the ground of anticipation.
3. The On-sale Bar and “Anticipation”
M3 Systems defends these anticipation verdicts by arguing that the asserted claims are anticipated because they are subject to an on-sale bar. Although 35 U.S.C.
Conclusion
In sum, M3 Systems directs us to no prior art or prior knowledge or use by others that constitutes substantial evidence of anticipation of the needles claimed in the ’056 patent. M3’s witnesses conceded that the ’056 needles differ from the Tru-Cut in the flange structure for coupling to the gun for movement both toward and away from the housing, a structure that limits all claims, as well as in the additional limitation in claims 10 and 12 of a slit in the stylet head flange. It is not disputed that the Tru-Cut needle assembly lacks these elements. In view of these admitted differences between the ’056 needles and the prior art, differences unambiguously stated in the ’056 claims, the verdicts of anticipation are unsupported by substantial evidence. The judgment of invalidity on this ground is reversed.
B. Obviousness
Invalidity based on obviousness is a question of law based on underlying facts. See Graham v. John Deere Co.,
The ultimate determination of obviousness vel non is a legal conclusion. See Ashland Oil, Inc. v. Delta Resins & Refractories, Inc.,
M3 Systems argued at trial that the patented needle assembly would have been obvious in light of the Tru-Cut needle assembly, and that the only differences arose from obvious adaptations to accommodate the new gun design and to provide the desired reverse movement of the needles. No other prior art was presented. The invention that was made, however, does not make itself obvious; that suggestion or teaching must come from the prior art. See, e.g., Uniroyal, Inc. v. Rudkin-Wiley Corp.,
No prior art provided a teaching or suggestion or motivation that a needle assembly should be made with the structure shown and claimed in the ’056 patent. Absent this essential evidentiary component of an obviousness holding, as a matter of law the verdicts of invalidity on that ground can not stand. Consequently, the judgment of invalidity based on obviousness is reversed.
C. Inventorship
The jury rendered special verdicts of invalidity of the asserted ’056 claims on the ground of incorrect inventorship. Inventor-ship is a question of law, applied to relevant facts. Findings of relevant fact are reviewed on the standard appropriate to the trier of fact, in this case for substantial evidence. See Hess v. Advanced Cardiovascular Sys., Inc.,
The “inventor,” in patent law, is the person or persons who conceived the patented invention. Collar Co. v. Van Dusen,
An assertion of incorrect inventor-ship must be based on facts proved by clear and convincing, corroborated evidence. Hess,
§ 256 Whenever through error a person is named in an issued patent as the inventor, or through error an inventor is not named in an issued patent and such error arose without any deceptive intention on his part, the Commissioner may, on application of all the parties and assignees, with proof of the facts and such other requirements as may be imposed, issue a certificate correcting such error.
See Stark v. Advanced Magnetics, Inc.,
The ’154 patent as filed in the United States had named Dr. Lindgren as sole inventor. In the course of the reissue proceeding Dr. Lindgren filed a petition in the PTO to add Dan Ákerfeldt as a joint inventor. Lindgren and Ákerfeldt each filed declarations explaining their roles in the invention and declaring that the omission in naming Ákerfeldt was due to differences between United States and Swedish patent law, and was not done with intent to deceive.
M3 Systems challenged the joint inven-torship of Lindgren and Ákerfeldt, and also stated that neither one was an inventor of the ’056 patent’s needles, but that Alan Taylor, President of Hart Enterprises, the company Radiplast retained to manufacture, its new needles in the United States, was the sole inventor. Although Mr. Taylor did not appear at the trial, he stated in a deposition that he was not an inventor, but that he suggested the slot in the stylet flange to cooperate with a guide pin in the gun and prevent rotation of the needle. He said he sketched his design for Mr. Engstróm, although such a sketch was not produced. M3 states that Mr. Taylor gave written notice of his claim in 1990, before the reissue application was filed, but the record citations in M3’s brief do not direct us to such notice.
It has long been the rule that one who asserts “inventor” status must provide clear and convincing evidence of supporting facts, including corroborating evidence. See Woodland Trust v. Flowertree Nursery, Inc.,
Alternatively, M3 Systems points to the design patents that were filed in the name of Ákerfeldt alone, as establishing that Dr. Lindgren was not a joint inventor of the needles with Ákerfeldt. Bard replies, and there is no dispute, that the design patents showed specific hub designs not shown in the utility patent. Whether Ákerfeldt was the sole inventor of specific hub designs does not negate his joint inventorship of the needles of the ’056 patent, which are depicted and claimed broadly. Bard also stresses that if indeed there were error in inventorship, such errors are correctable and do not invalidate the patent absent deceptive intent. To invalidate a patent based on incorrect inventor-ship it must be shown not only that the inventorship was incorrect, but that correction is unavailable under section 256:
§ 256 [¶ 2] The error of omitting inventors or naming persons who are not inventors shall not invalidate the patent in which such error occurred if it can be corrected as provided in this section....
Although M3 contends that deceptive intent can be inferred from the omission of Taylor as an inventor, precedent requires that one who claims a share of inventorship must establish that right by clear and convincing evidence. Ethicon,
D. Violation of Reissue Requirements
The jury also found by special verdicts that the asserted ’056 claims were invalid on
With respect to the argument that the correction of inventorship was improperly made by reissue, we have been directed to no legal or procedural error, for the prosecution history clearly shows that the error in inventorship was described in the reissue application and corrected by appropriate petition, filed and processed while the reissue application was pending. A petition to correct inventorship, 37 C.F.R. § 1.324 (1991), may be filed during reissue proceedings. The error in inventorship was corrected before the reissue patent was granted, and thus the reissued patent names Lindgren and Ak-erfeldt as the inventors. This procedure can not have provided ground for a reasonable jury’s verdicts of invalidity based on violation of reissue requirements.
The other aspect that M3 Systems argued was not amenable to correction by reissue was the addition of claims to the needles per se. That argument incorrectly states the reissue law, for a primary purpose of the reissue statute is to enable the addition of claims to subject matter not claimed in the original patent. See Scripps Clinic & Res. Found’n v. Genentech, Inc.,
M3 Systems states that since the needles were not claimed originally they were not “intended” to be claimed, and that absence of such intent is not an error correctable by reissue. That too is an incorrect statement of the law. An inventor’s failure to appreciate the scope of an invention at the time of the original patent grant, and thus an initial intent not to claim the omitted subject matter, is a remediable error. See In re Amos,
M3 Systems also argues that the error in failing to claim the needles should have been corrected sooner. The reissue statute sets a two-year time limit for filing a broadening reissue application. This requirement was met. See 35 U.S.C. § 251; In re Graff,
M3 Systems has stated no basis in fact or law for its assertion that any reissue procedure was violated. The verdicts of invalidity on this ground are unsupported in law, and judgment based thereon is reversed.
E. The On-Sale Issue
The jury also found that the asserted ’056 claims were invalid on the ground that the new needle assembly had been “patented or published or in public use or on sale” in the United States more than one year before the
Although the special verdicts did not distinguish among the statutory grounds of patented or published or in public use or on sale, the major focus at trial and on appeal is the issue of on sale. While M3 Systems also argued that there was a bar based on publication and public use, the only evidence referred to relates to the first generation gun and the Tru-Cut needles, which are acknowledged prior art and are not claimed in the patents in suit. M3’s argument at trial that these prior art devices were also a bar to the ’056 claims under section 102(b) is not pressed on appeal.
The ’154 and ’056 patents are directed to the second generation gun and new needles. Before the critical date, indeed before the development of the second generation gun and new needles had been completed, Radi-plast was engaged in a variety of activities directed to the United States market. These activities included demonstrating and promoting the first generation gun with the Tru-Cut needles, pursuing arrangements for clinical trials for the second generation gun and new needles through collaboration with a potential United States distributor, applying for FDA approval, arranging for manufacture of the needles in the United States, and related activities directed to commercial goals. Although Radiplast’s final needle design was developed after the critical date, the issue at trial was the effect of these prior activities under the law of section 102(b).
Federal Circuit precedent on the on-sale bar requires consideration by the court of the totality of the circumstances in light of the various policies that underlie the bar. Precedent explains that “while a wide variety of factors may influence the on sale determination, no single one controls the application of section 102(b), for the ultimate conclusion depends on the totality of the circumstances.” Ferag AG v. Quipp, Inc.,
Although a few cases have recognized the advantages of a bright line rule that would be applicable in all eases, that is, a defining event whereby an inventor will know when the bar will accrue, generally the court has undertaken to weigh the particular facts of the commercial activity against the particular policy considerations that apply to the situation, giving effect to the principle that “the policies or purposes underlying the on sale bar, in effect, define it.” RCA Corp. v. Data General Corp.,
The determination of whether a product was on sale in terms of section 102(b) is a question of law. See Micro Chem., Inc. v. Great Plains Chem. Co.,
The various policy considerations include the policy of providing a limited but normally sufficient time (one-year) for the inventor to
Before the critical date for the ’056 patent, July 30, 1985, three sets of events were explored at trial. The facts are not in dispute; the question is whether, as a matter of law, the on-sale bar arose in these circumstances:
1. The Clinical Trials
The clinical trials were arranged by American Pharmaseal, Radiplast’s potential distributor in the United States, and were conducted in August and September 1985 (after the critical date) using the second generation guns and new needles. In January 1985 Thomas Engstrom of Radiplast had quoted to Pharmaseal the price for 12 guns and 500 needles for use in the trials. Pharmaseal later that spring requested 10 guns and 250 needles, for which Radiplast sent an invoice in June 1985. Mr. Engstrom testified that this payment was to defray some of Radi-plast’s costs in providing these devices, and was so understood. It was not disputed that the transaction produced no profit for Radi-plast.
M3 Systems asserts that Radiplast sold the 10 guns and 250 needles to Pharmaseal, pointing out that a standard sales invoice was used. Bard replies that this was a transaction between collaborators, not a commercial sale and not a sale for commercial distribution. Dr. Lindgren testified that he visited the four United States hospitals that were testing the device (after the critical date), to explain its use and to see how it worked in different tissues, operated by different doctors. Bard stresses that the devices were not sold, that all but one were returned by the hospitals after the clinical trials, and unused needles were destroyed.
Generally cost defrayal arrangements between collaborators are not deemed to be invalidating sales, nor are payments for use substantially for test purposes. See In re Mahurkar,
It is not disputed that the sole purpose of this transaction was to make the devices available to the four selected hospitals for a limited test period. Radiplast’s arrangement with Pharmaseal for payment or defrayal of the cost of providing the devices was not a sale or offer of sale as contemplated by section 102(b). It contravenes none of the policies underlying the on sale bar for Radiplast to have recouped these costs. Upon considering the totality of the circumstances, I conclude that an on-sale bar did not arise based on this transaction between Radiplast and Pharmaseal in connection with the clinical trials.
In January 1985 Radiplast quoted to Phar-maseal prices for various bulk quantities of up to 50,000 needles. At that time the new needles were still being modified, and the record shows that design changes were made well after January 1985. Mr. Engstrom of Radiplast testified that the quotation was information for a potential distributor, in the event that Pharmaseal accepted that role (it did not). The bulk price quotations were in a telex that stated, “This is to give you an indication of the price levels. We have to meet and discuss more in detail all things related with the marketing of our biopsy instrument in US.” It was not disputed that the quotation was for modified needles, and that both parties understood that the modified needles were not yet available.
M3 Systems argues that since the first generation device had been shown to operate for its intended purpose using Tru-Cut needles, the inventor had already convinced himself that he had a satisfactory product that he wished to commercialize in the United States, and thus that the bulk price quotation, even if for needles not yet developed, was an on-sale event. M3 stresses that the price quoted for bulk quantities included a profit for Radiplast, unlike the price for the clinical trial quantities.
Quotation of a sales price to a potential distributor of a product that is not available for sale and distribution does not of itself establish an on-sale bar. See Continental Can,
In this case, the circumstances of the incomplete stage of development of the second generation gun and proposed new needles at the time of this price quotation, the potential but not established distributor relationship underlying this quotation, the planned clinical collaboration, and the non-existence of a completed final product, negate the accrual of an on-sale bar from this price quotation. It seems clear that neither Radiplast nor Pharmaseal expected that this bulk price quotation would be followed by the placement of an order. To satisfy the on-sale requirement of section 102(b) there must be more than an informational exchange of price information, when there is no reasonable contemplation that the quotation will be followed by purchase and sale as a commercial transaction.
I conclude that the verdicts of invalidity based on the on-sale bar can not be supported by this bulk price quotation.
3. The Correspondence with Dr. Phelps
The third event raised by M3 Systems occurred in November 1984. Mr. Engstrom of Radiplast responded to a letter written in September 1984 by Dr. Phelps, a physician in Alabama, who had seen a demonstration and brochure for the first generation device and wrote to Sweden for information. Engstrom wrote back that he hoped to start marketing a second generation device and new needles in the United States in early 1985, and that if Dr. Phelps did not wish to wait until United States distribution was arranged he could
An offer of sale originating in a foreign country, (Erected to a consumer in the United States, can establish an on-sale bar as to what was offered. In re Caveney,
At the time of Mr. Engstrom’s letter the second generation device and needles were in an early development stage. Although Dr. Phelps was not told the details of these developments, this correspondence did not raise an on-sale bar to a product not yet developed. As held in Robotic Vision Sys., Inc. v. View Eng’g, Inc.,
Upon de novo review of the totality of the circumstances, with due consideration to the applicable policies, the undisputed facts, and drawing factual inferences in favor of the verdicts, I conclude that the verdicts of invalidity based on a section 102(b) bar are incorrect; I would reverse the judgment on that ground.
II
INFRINGEMENT OF THE ’056 PATENT
In view of the majority’s affirmance of the judgment of invalidity, we do not reach the issue of infringement of the ’056 patent. That judgment is vacated.
VALIDITY OF THE ’308 PATENT
The ’308 patent is directed to the third generation gun. The jury found the asserted claims of the ’308 patent not infringed, and invalid or unenforceable on the grounds of anticipation,' obviousness, and insufficient supporting description, as well as for fraud, misuse, and violation of antitrust law, as discussed in Parts V-VII, post.
Claims 15 and 16 were at issue, with emphasis added to show the claim terms whose construction is relevant to the issues of patent validity or infringement:
15. A tissue sampling device comprising:
a guide sleeve having front and rear guide sleeve ends and defining a longitudinal axis extending between said front and rear guide sleeve ends, said front guide sleeve end having an opening there-through;
a hollow first needle positioned within said guide sleeve and extendable from said opening, said hollow first needle being moveable along said axis;
a second needle extending through said hollow first needle and moveable along said axis, said second needle having a tip which is extendable from said hollow first needle and said opening, and said second needle further including a tissue sample receiving recess;
a first needle head coupled to said hollow first needle and mounted within said guide sleeve for movement along said axis to move said hollow first needle along said axis;
a second needle head coupled to said second needle and mounted within said guide sleeve for movement along said axis to move said second needle along said axis;
a first spring disposed within said guide sleeve and operatively associated with said second needle head, said first spring being capable of being placed into an energized mode to store energy, and said first spring being releasable from said energized mode to propel said second needle head along said axis towards said opening, such that said tip of said second needle is extended from said hollow first needle, whereby a tissue sample can be captured within said recess;
a second spring positioned within said guide sleeve and operatively associated with said first needle head, said second spring being capable of being placed into an energized mode to store energy, and said second spring being releasable from said energized mode to propel said first needle head along said axis towards said opening, said hollow first needle being extended from said opening such that said recess of said second needle is enclosed by said hollow first needle;
a first latch means selectively releasable from outside said guide sleeve for releas-ably holding said first spring in said energized mode;
a second latch means for releasably holding said second spring in said energized mode, said second latch means being releasable in response to and subsequent to release of said first spring; and
sequential energizing means operative to move said first needle head along said axis towards said rear guide sleeve end to cause said second latch means to hold said second spring in said energized mode, and subsequently to move said second needle head along said axis towards said rear guide sleeve end to cause said first latch means to hold said first spring in said energized mode.
Claim 16 is the same as claim 15 except for the last clause, which includes the selective retraction of the stylet to expose the tissue sample:
16. energizing means operative to move said first needle head and said second needle head along said axis towards said rear guide sleeve end to cause said first latch means to hold said first spring in said energized mode and to cause said*1360 second latch means to hold said second spring in said energized mode, said energizing means being selectively operative to move said first needle head but not said second needle head towards said rear guide sleeve end, whereby said hollow first needle is selectively retractable to expose said tissue sample receiving means in said second needle.
A. Support by the Written Description
The jury found claims 15 and 16 “not supported by the description contained in the specification.” M3 Systems explains that the issue was the meaning of the claim terms “sequential energizing” and “energizing means.” The district court had permitted the jury to resolve this disputed issue of claim construction. On this appeal we give de novo review to the issues relevant to the construction and interpretation of the claims. See Cybor,
M3 Systems states that “sequential” should be construed, and was construed by the jury, to permit no overlap of needle movement during the energizing step. M3 states that since the patent shows that the second needle can start to move before the first needle has completed its movement, the written description does not support the claims. M3 states, as it did at trial, that since the specification does not describe how to obtain elimination of all overlap of needle movement, the claims are not supported by the written description and are invalid.
Bard agrees that the specification shows a slight overlap in the movement of the needles, whereby the second needle starts to move just before the first needle has completed its movement and the first spring latches. Thus, Bard contends, correct interpretation of the claims allows for this slight overlap in needle movement. Bard states that it is incorrect to construe the claims contrary to the specification, and then to hold the claims invalid because they are contrary to the specification. Bard is of course correct; the claims are construed in accordance with the rest of the specification of which they are a part, and not contrary to it. See Slimfold Mfg.,
The specification illustrates the sequential energizing of the needles as having some overlap in movement of the needles. The term “sequential” in the claims is in accordance with this description in the specification; no usage or exemplification of the sequential movement requires eliminating all overlap. It is incorrect to construe the claims as barring all overlap, as urged by M3 Systems. On the correct claim construction, no reasonable jury could have found that the claims are not supported by the description in the specification. It is thus apparent that the jury either adopted M3’s erroneous claim construction, or incorrectly applied the law governing claim construction to the undisputed facts of the structure described in the specification.
On the correct claim construction the written description is in accordance with and in support of the claims. The judgment of invalidity on this ground is reversed.
B. Anticipation
The jury also found claims 15 and 16 invalid based on anticipation. “Anticipation” requires that the identical invention was already known to others, that is, that the claimed invention is not new. See Minnesota Mining & Mfg. Co. v. Johnson & Johnson Orthopaedics, Inc.,
Indeed, the jury verdicts can be understood only if one adopts so tortured a.view of the law. As we have discussed, it is incorrect to construe claims contrary to the specification, and it is incorrect to construe terms in means-plus-function form as disembodied from the structure in the specification. M3 Systems’ witnesses readily admitted that the integrated mechanized gun described and claimed in the ’308 patent is different from the first generation gun and the description of that gun in the PCT application. On the undisputed facts and the correct law, a reasonable jury could not have found the ’308 claims anticipated thereby. The judgment of invalidity for anticipation must be reversed.
C. Obviousness
M3 Systems argues that the third generation gun of the ’308 patent would have been obvious in view of the PCT application and the first generation gun, in combination with the ’154 patent describing the second generation gun. M3 states that the third generation is an obvious combination of elements found in the first and second generations. See discussion, Part I.B. ante, of the law of obviousness. There was no dispute as to the scope and content of this prior art, or as to the elements in the third generation gun that were not in either the first or second generations. The only dispute was the ultimate question of whether the third generation gun would have been obvious from what had gone before.
M3 Systems contends that for the third generation the inventor simply changed the integrated mechanical cocking mechanism of the second generation gun to accomplish mechanically the sequential cocking that was necessarily done when the first generation gun was manually cocked, one spring at a time. Bard replies that the one-at-a-time cocking of the springs in the first generation, by hand or by miniature crowbar, does not teach or suggest the integrated automatic sequential cocking of the third generation, and that there is no teaching or suggestion in the prior art to make such a combination, or of the structure having the improved ease of handling of the third generation gun. Bard also points to the other new structural features of the third generation whereby the needles can be retracted separately after tissue sampling.
The ultimate question is whether, from the evidence of the prior art and the knowledge generally available to one of ordinary skill in the relevant art, there was in the prior art an appropriate teaching, suggestion, or motivation to combine components in the way that was done by the inventor. See, e.g., Uniroyal,
Bard points out that its rotating sleeve mechanism for sequential energizing is a marked distinction from its earlier devices, even were the concept of sequential energizing deemed to be derivable from the manual operation of the first generation. M3 Systems does not cite any reference suggesting the structure employed in the third generation gun, or any suggestion of mechanical sequential energizing, or indeed the other features of the third generation. Those contributions came from the inventor, not the prior art. See Uniroyal,
TV
INFRINGEMENT OF THE ’308 PATENT
The jury found that M3 Systems did not infringe claims 15 and 16 of the ’308 patent. Because the special verdicts discussed in Part III A (that there is not support for these claims in the written description) require an incorrect claim construction, we have reviewed the verdicts of noninfringement on the correct construction, i.e., that claims 15 and 16 do not require a total absence of overlap in the sequential movement of the needles during energizing. Bard contends that on the correct claim construction the verdicts of noninfringement can not stand. Bard is entitled to a new trial if a jury reasonably could have reached verdicts of infringement upon correct claim construction and correct application of the law of infringement. However, if only one result is supportable in law and on undisputed facts, judgment as a matter of law is appropriate. See Strattec,
On appeal Bard argues only the issue of sequential energizing, asserting literal infringement under section 112 paragraph 6. M3 Systems does not dispute, and indeed emphasizes, that in its ProMag devices there is sequential energizing with a slight overlap in needle movement. However, M3’s performance of the function of sequential energizing was not the only disputed issue with respect to infringement. M3 also points out that its device is a box-type biopsy gun and does not contain a “guide sleeve” as required by the claims, and that the M3 ProMag guns use linear tensioning whereas the ’308 device performs counter-rotational tensioning, such that the structure used by M3 is not equivalent to that shown in the ’308 specification, applying section 112 paragraph 6 to the energizing means of the ’308 claims.
M3 Systems states that the ’308 patent draws a distinction between box-type biopsy guns such as those made by M3 wherein the housing is merely a container for the device, and guns embodying a mechanism wherein the guide sleeve and a tensioning sleeve interact and serve as part of the cocking mechanism. M3 argued at trial that its housing is independent, whereas in the '308 specification the gun is housed in a two-part structure wherein the inner part is the guide sleeve and the outer part is the tensioning sleeve and rotates about the inner part. These sleeves bear cam surfaces and slots that interact with the flanges on the needle heads and thus serve as part of the cocking mechanism. M3 states that its gun has neither a guide sleeve nor a tensioning sleeve, and that its housing is merely the container for the device, and is unconnected with the cocking mechanism.
Although the claims in suit do not require a tensioning sleeve, see D.M.I., Inc. v. Deere & Co.,
At the trial the parties presented evidence on how the patented and accused devices worked, and the court instructed the jury as to the applicable law of infringement of means-plus-function claims. For the energizing means Bard was required to establish, by a preponderance of evidence, that M3 Systems’ device embodies the structure described in the ’308 specification or an equivalent thereof. 35 U.S.C. § 112 ¶ 6; Valmont Indus., Inc. v. Reinke Mfg. Co.,
There was no dispute that the function of sequential energizing is performed in the M3 Systems’ guns; the only question was whether the M3 guns employ the same or an equivalent of the structure described in the ’308 specification. The accused equivalent structure need not have been known at the time the patented invention was made. See Texas Instruments,
It was explained at trial that to achieve sequential energizing in the ’308 device the outer tensioning sleeve is rotated about the inner guide sleeve; cam surfaces on the interior of the tensioning sleeve push against wings built directly into the needle heads to compress the two springs in sequence, pressing them rearward into the locked position. In contrast, in the M3 Systems device a handle connected through the rear of the housing acts on sleds bearing the needles; M3’s device relies on the lever-action of the handle, as opposed to a rotating sleeve, to pull, rather than push, the needle sleds sequentially back toward their respective latches. Bard had argued at trial, in connection with the issue of validity, that the claims “must be interpreted as means-plus-function terms in accordance with Valmont,” and cited its “external integrated energizing mechanism that converts rotary motion to linear motion” to distinguish the ’308 gun from its own earlier device. Claims must be interpreted the same way for determining infringement as was done to sustain their validity.
A reasonable jury could have found that the structure using rotational tensioning as the energizing means is substantially different from the energizing structure in the M3 Systems guns. Although Bard argues that it suffices for infringement if the energizing is achieved with the slight overlap shown in the ’308 patent, that is, if the function of sequential energizing is performed, claims written in the form authorized by section 112 paragraph 6 are limited by the structure described and equivalents of that structure. Performance of the same function does not of itself establish infringement.
Bard directs us to the doctrine of claim differentiation, and argues that it is incorrect to interpret the “sequential energizing means” of claim 15 as limited to the structure in the specification, because other claims, not at issue, specifically state that structure. Bard argues that its claims in suit are broad
Applying this law, and based on the absence of a guide sleeve or any counterpart structure, and the differences in the structures of the energizing mechanisms, we conclude that on the correct claim interpretation a reasonable jury could find that claims 15 and 16 are not infringed. The judgment of noninfringement of the ’308 patent is affirmed.
V
FRAUD
M3 Systems charged that Bard had committed both fraud and inequitable conduct in prosecuting the ’056 and ’308 patents. The jury was not asked to decide the issue of inequitable conduct, which was reserved to the judge and withdrawn by M3 after the favorable verdicts on the question of fraud. The jury found that it had been established by clear and convincing evidence that each of the ’056 and the ’308 patents had been procured by fraud in the Patent and Trademark Office.
Fraud in the procurement of a patent requires proof of the elements of fraud as developed in the common law: (1) that a false representation of a material fact was made, (2) with the intent to deceive, (3) which induced the deceived party to act in justifiable reliance on the misrepresentation, and (4) which caused injury that would not otherwise have occurred. See Nobelpharma AB v. Implant Innovations, Inc.,
The tort of fraud requires that there was a successful deception, and action taken by the person deceived that would not have otherwise been taken. Applied to patent prosecution, fraud requires (1) a false representation or deliberate omission of a fact material to patentability, (2) made with the intent to deceive the patent examiner, (3) on which the examiner justifiably relied in granting the patent, and (4) but for which misrepresentation or deliberate omission the patent would not have been granted. A finding of fraud can of itself render the patent unenforceable, and when accompanied by the elements of violation of the Sherman Act, as discussed iri Part VI, can incur additional consequences.
To establish fraud for purposes of antitrust violation the defendant “must make a greater showing of scienter and materiality” than when seeking unenforceability based on conduct before the Patent Office. 6 Donald S. Chisum, Chisum on Patents § 19.03[6][e] (rel. 47 1993) (citations omitted). In Walker Process Equip., Inc. v. Food Mach. & Chem. Corp.,
M3 Systems stated that Bard made myriad material misrepresentations in prosecuting the ’056 and the ’308 patents, including the following: the incorrect inventors were named; actual samples of the TruCut needles and the first generation device were not provided to the examiner; the Baxter patent on the Tru-Cut needle and two Lindgren articles on the first generation device were not provided to the examiner; the material submitted to the FDA was not provided to the examiner; the examiner was not told of the eo-pending design patents; and the examiner was not provided with all of the evidence on the on-sale issue. Bard responded that there is no substance to any of these assertions; that all material information was presented to the examiner; that there was no intent to deceive the examiner; that the examiner was not deceived; and that the evidence points to good faith in the prosecution of these patents. Good faith is an absolute defense to the charge of common law fraud. See Walker Process,
M3 Systems argues that any omission in the submissions to the PTO is “necessarily material, because the allowance of the application is the intended natural consequence of that submission.” That is not a correct statement of the law. There is no presumption that information not filed by an applicant was material simply because patentability ensued. To establish culpability any omission must be of a fact material to patentability and it must be a deliberate misrepresentation, whether by omission or misstatement, that was intended to and did mislead the examiner into taking favorable action that would not otherwise have been taken. Intent to mislead or to deceive must be proved by clear and convincing evidence. See Walker Process, supra. Deceptive intent is not inferred simply because information was in existence that was not presented to the examiner; and indeed, it is notable that in the usual course, of patent prosecution many choices are made, recognizing the complexity of inventions, the virtually unlimited sources of information, and the burdens of patent examination. See Northern Telecom,
Following are the actions that M3 Systems presented as probative of fraud in the prosecution of the ’056 or the ’308 patent:
1. The Inventorship Issue
This issue was discussed ante in connection with the validity of the ’056 patent. There was no evidence of intent to deceive in correcting the inventorship to include Mr. Akerfeldt with Dr. Lindgren as joint inventors. The question of Mr. Taylor’s role as a possible inventor did not present substantial evidence of fraud. Indeed, since the inven-torship issue was not grounds of invalidity, it can not satisfy the “but for” test of fraud.
2. Provision of Actual Models to the Examiner
M3 Systems argued that Bard should have provided the reissue examiner with actual models of the first generation gun and the Tru-Cut needles, in addition to the PCT application and publications describing the needles. The PCT application described the first generation gun, and descriptions of the Tru-Cut needles were before the examiner. Reviewing the prosecution history we do not discern substantial evidence of material withholding, for cumulative information is not material to patentability, and there was no evidence of deceptive intent or that the examiner was deceived into granting the reis
3.Provision of On-Sale Information to the Examiner
Bard filed with the PTO descriptions of the transactions involving Radiplast and Pharma-seal before the critical date, accompanied by documents including the invoice for the 10 guns and 250 needles for the clinical trials, the bulk price quotation discussed ante in connection with the on-sale issue, and declarations concerning the hospital tests and the proposed distribution relationship between Radiplast and Pharmaseal. M3 Systems states that Bard should have also disclosed to the PTO Radiplast’s sales activities for the first generation device, Radiplast’s letters to doctors concerning the clinical trials, the fact that the bulk price quotation included a profit, and Radiplast’s letter to Dr. Phelps.
Concerning Dr. Phelps, Bard answers that it submitted to the PTO all the relevant material it had obtained. The letter to Dr. Phelps was obtained after suit was filed, during discovery of Radiplast’s files in Sweden. There was no evidence that Bard had obtained and withheld this information during the reissue prosecution. With respect to the bulk price quotation, M3 Systems states that Bard should have flagged this document and described its significance to the examiner, lest it be overlooked in the volume of paper. Bard responds that the documents provided to the examiner were a record of Radiplast’s efforts to find a distributor and its transactions with Pharmaseal, and that the total number of documents was not so voluminous, or the contents so difficult to understand, as to support an inference of intentional concealment of any particular document that was filed. We agree that these documents, all in the prosecution history, are easily read.
On reviewing these filings in the PTO we have been directed to no evidence of material withholding or the provision of false information, or of intent to deceive or actual deception. The additional subject matter that M3 states should have been included was not shown to be material or other than cumulative. These actions did not constitute substantial evidence of fraud.
4. Disclosure of the Information Filed with the FDA
None of the material provided us with respect to Radiplast’s 510(k) pre-market notification filed with the Food & Drug Administration supports a finding of fraud in the patent prosecution. M3 Systems concentrates on the presence in this package of needle drawings made by Hart Enterprises, the designated manufacturer. As we have explained, the inventorship issues that have been raised do not provide substantial evidence of fraudulent procurement of these patents.
5. Disclosure of the PCT Application
The PCT application had been submitted to the PTO during prosecution of the ’154 patent and again during the ’056 reissue proceedings. M3 Systems states that Bard withheld the PCT application from the examiner of the ’308 patent and then miseharac-terized it.
M3 Systems stated at trial and repeats on this appeal that Bard submitted the PCT application to the examiner of the ’308 patent only after allowance of the ’308 claims in suit, and then falsely represented that it was relevant solely to newly added claims 21-23 (as then numbered). Bard complains that M3 misstated at trial, and continues to misstate, these facts. We must agree. The ’308 prosecution history in the record shows that Bard cited the PCT application and filed a copy thereof with a Supplemental Information Disclosure Statement accompanying Bard’s first response, filed October 13, 1989, to the
In submitting the PCT Application Bard’s patent attorney pointed out the aspect of that application that M3 Systems has stated is of greatest significance, viz., the separate and thus sequential hand cocking of the springs in the first generation device. In the Remarks section of the response Bard discussed claims 21-23, the claims specific to sequential energizing. We discern no support for M3’s argument that Bard misrepresented the content of the PCT application, or that the examiner did not consider the PCT application adequately. The examiner initialed on December 15, 1989 that he had considered this reference, the same day a telephone interview was held that led to an examiner’s amendment, followed by allowance on January 3, 1990. The charge of fraud based on these events is totally without substance.
Conclusion
These asserted flaws in patent prosecution, separately or taken together, do not constitute substantial evidence of fraud. The verdicts of fraud in procuring the ’056 and ’308 patents can not stand, and the judgment on these verdicts is reversed.
VI
ANTITRUST ISSUES
Antitrust violation was found on special verdicts that Bard by anticompetitive conduct had monopolized or attempted to monopolize the relevant markets for each of fully automated biopsy guns and needles, guns alone, and replacement needles. The jury instructions on the antitrust count identified three separate claims; first, that the patents were procured by fraud followed by attempts to enforce the fraudulently procured patents; second, that Bard threatened and then brought suit knowing that its patents were invalid, unenforceable, or not infringed; and third, that Bard unlawfully leveraged its monopoly power in the guns to obtain a competitive advantage in replacement needles by modifying its gun to accept only Bard needles. The jury found in favor of M3 Systems and against Bard on every question, and assessed compensatory damages, measured primarily as litigation costs, of $1.5 million, which were trebled as required by section 4 of the Clayton Act. Bard argues that the findings are not supported by substantial evidence, and that judgment as a matter of law should have been granted.
A. The Walker Process Claim
Fraud in obtaining a United States patent is a classical ground of invalidity or unenforceability of the patent. In Walker Process,
The jury found by special verdicts that the ’056 and ’308 patents were obtained by fraud in their prosecution before the PTO, as discussed in Part V, ante. The jury also
It is not presumed that the patent-based right to exclude necessarily establishes market power in antitrust terms. See Abbott Labs. v. Brennan,
Thus it was necessary for M3 Systems to establish market power as well as fraudulent procurement of the patent and that Bard’s related commercial activity was coupled with violations of section 2. In addition, applying the law of the Seventh Circuit to the elements of section 2, M3 was required to establish that Bard had a specific intent to monopolize, engaged in anti-competitive conduct, and had a dangerous probability of success. See Great Escape, Inc. v. Union City Body Co.,
B. “Sham” Litigation
Conduct prohibited under antitrust law includes bringing suit to enforce a patent with knowledge that the patent is invalid or not infringed, and the litigation is conducted for anti-competitive purposes. In such events the antitrust immunity of Noerr-Pennington and California Motor Transp. Co. v. Trucking Unltd.,
The Supreme Court in Professional Real Estate Investors, Inc. v. Columbia Pictures Indus., Inc. (PRE) established the two-part criteria of “sham” litigation: (1) the lawsuit must be objectively meritless such that “no reasonable litigant could expect success on the merits” and (2) it must be found that “the baseless lawsuit conceals ‘an attempt to interfere directly with the business relationships of a competitor.’ ”
Thus although sham litigation as a tactic to destroy competition can lead to antitrust violation, see U.S. Philips Corp. v. Sears Roebuck & Co.,
Neither the bringing of an unsuccessful suit to enforce patent rights, nor the effort to enforce a patent that falls to invalidity, subjects the suitor to antitrust liability. Cf. Concrete Unltd. Inc. v. Cementcraft, Inc.,
M3 Systems states that Bard knew its patents were not infringed when it brought suit, citing the testimony of a Bard engineer that he did not think the original M3 needle infringed the ’056 patent and that other Bard employees had told him that M3 changed its needle design to one that did not infringe. The engineer also testified that he did not know whether those who told him M3’s needles did not infringe had ever read the ’056 patent, or whether they were familiar with the concept of infringement under the doctrine of equivalents. This was the totality of the evidence of sham litigation concerning the ’056 patent; there was no evidence at all with respect to the ’308 patent.
C. Attempt to Monopolize
M3 Systems proposed that Bard had modified its biopsy gun and needles for the purpose of preventing use of Tru-Cut needles and then to exclude M3’s copies so that they did not fit the gun without an adapter. M3 contends that Bard’s motives were anti-competitive, pointing to Bard documents showing internal discussions of competitive products and concern for patent scope and market share. Bard replies that the Tru-Cut was not suitable for its new gun because it could not achieve reverse motion, and points out that M3’s witness acknowledged that M3 could effectively compete, as were several other producers of biopsy guns and needles.
Bard was under no duty to facilitate M3’s competition by refraining from changing its products. The jury instructions did not distinguish patent-supported products and markets based thereon from actions described to the jury as being in restraint of trade. For example, the jury instruction on intent to monopolize was as follows:
M3 Systems also alleges that it was injured by Bard’s unlawful attempt to mo*1370 nopolize. An attempt to monopolize may be proven even if Bard lacks monopoly power, but because of its alleged exclusionary conduct, there exists a dangerous probability that Bard will obtain monopoly power in any market. In order to win on its claims of attempted monopolization, M3 Systems must prove each of the following elements by a preponderance of the evidence:
First, that Bard had a specific intent to achieve monopoly power in a relevant market; second, that Bard engaged in exclusionary or restrictive conduct in furtherance of its specific intent; third, that there was a dangerous probability that Bard would obtain monopoly power in the relevant market; and, fourth, that M3 Systems was injured in its business or property by Bard’s conduct.
In explaining further, the district court referred to “exclusionary or restrictive conduct” and “unreasonable acts and practices,” again without reference to patented products and their status in the law. Although the court instructed that “conduct that involves the introduction of superior products” is not exclusionary or ■ restrictive, the court also stated that “where conduct is ambiguous, direct evidence of a specific intent to monopolize may lead you to conclude that the conduct was intended to be and was in fact exclusionary or restrictive.” No mention was made of the patentee’s statutory right to exclude, and there was no instruction to consider that right.
These broadly stated descriptions of exclusionary or restrictive conduct, unlimited by the conditions set in Walker Process or PRE and taking no cognizance of the legal rights of the patent grant, do not rise to the level of violation of antitrust law. Thus I must, respectfully, dissent from the court’s ruling that Bard incurred liability under the Sherman and Clayton Acts by its actions in modifying and improving its patented products, thereby requiring M3 to provide an adapter with its replacement needles for the Bard gun.
The panel majority on this issue holds that the jury verdict of monopoly power must be sustained, although the power held by Bard in this market is based on the patent right. Bard or its predecessor Radiplast changed from the Tru-Cut to a newly designed needle that was capable of reverse movement, thus facilitating removal, inspection, and reinsertion of the inner needle while the cannula remained in place. This needle assembly is the subject of the ’056 patent. The record states that M3 was obliged to use an adapter to fit its existing needles to Bard’s gun; that is the antitrust ill of which M3 complained. This does not, as a matter of law, present a jury question of violation of the Sherman Act. See California Computer Prods., Inc. v. International Bus. Mach. Corp.,
Both the needle assembly alone and the integrated biopsy gun/needle device were patented. They were subject to Bard’s patent-based rights to exclude others from making, using, or selling them. It was not Bard’s changes to its biopsy gun or needles that affected M3’s sale of replacement needles; it was the patents on these products. To hold that Bard could violate the Sherman Act by changing these products, if M3’s business was adversely affected, is a novel and pernicious theory of antitrust law that is contrary to the principles of competition, and fraught with litigation-generating mischief.
Despite this court’s recent affirmation in Virginia Panel Corp. v. MAC Panel Co.,
The concept that antitrust law should bar an innovator from making changes or improvements to its products, when others may be affected thereby, is not brand new. However, cases where this issue has been litigated have been of a different order of competitive impact than here asserted; and I have found no case in which such a charge has been sustained. In In re IBM Peripheral EDP Devices Antitrust Litig.,
A basic premise of patent law, and antitrust law in general, is that the commercial advantage gained by new technology, and its statutory protection by patent, do not convert the possessor thereof into a prohibited monopolist. In United States v. Grinnell Corp.,
When the market for new technology is protected by patent, to violate the antitrust law there must be an improper use of the patent right, “coupled with violations of § 2.” Walker Process,
M3 did not allege the elements of an antitrust violation when patents are involved. See, e.g., Double D Spotting Service, Inc. v. Supervalu, Inc.,
I need not elaborate on the litigation opportunity affecting innovation-based industry, that is here so casually enabled. “Where competitors’ products must interface with the monopolist’s product the monopolist’s intro
The proceedings at trial, and the jury instructions, made no mention of the patent rights here present. It is without precedent to find antitrust liability premised on a theory that development of new products is illegally anticompetitive when the new product requires competing suppliers to adjust their product accordingly. Commentators who have considered the question of “whether product innovation can ever be unlawfully ‘predatory’ ” have concluded that “no admin-istrable rule could be fashioned that would not exact an unreasonably heavy toll.” 3 Phillip E. Areeda & Herbert Hovenkamp, Antitrust Law § 705b (rev. ed.1996). If this court deems it appropriate to add this burden to patent-based innovation, there should at least be some overriding public benefit. However, antitrust jurisprudence has well understood that the enforcement of the antitrust laws is self-defeating if it chills or stifles innovation. See IBM Peripheral, supra.
Neither the jury instructions nor the special interrogatories framed a charge of predatory conduct that comports with established criteria of antitrust liability. It appears that this charge at trial was cobbled together from left-over allegations of bad acts by bad actors. Indeed, M3’s antitrust counterclaims mention only Walker Process fraud and sham litigation, which all members of this panel agree were not established. I can not discern, in the law or in the record of this case, either legal or factual support for this new form of antitrust liability.
VII
MISUSE; OTHER ISSUES
The defense of patent misuse arises from the equitable doctrine of unclean hands, and relates generally to the use of patent rights to obtain or to coerce an unfair commercial advantage. Patent misuse relates primarily to a patentee’s actions that affect competition in unpatented goods or that otherwise extend the economic effect beyond the scope of the patent grant. See Mallinckrodt, Inc. v. Medipart, Inc.,
Patent misuse is viewed as a broader wrong than antitrust violation because of the economic power that may be derived from the patentee’s right to exclude. Thus misuse may arise when the conditions of antitrust violation are not met. See Zenith Radio Corp. v. Hazeltine Research, Inc.,
The jury returned special verdicts that Bard had misused both the ’056 and ’308 patents. Patent misuse arises in equity, and a holding of misuse renders the patent unenforceable until the misuse is purged; it does not, of itself, invalidate the patent. See Morton Salt Co. v. G.S. Suppiger Co.,
The jury instruction on patent misuse was focussed primarily on the charge that Bard was attempting to enforce the patents against goods known not to be infringing, the court explaining that antitrust violation is not necessary to find misuse if patents have been used “wrongfully” to exclude competitors:
A patent is unenforceable for misuse if the patent owner attempts to exclude products from the marketplace which do not infringe the claims of the patent and the patent owner has actual knowledge that those products do not infringe any claim of the patents. The patent is also unenforceable for misuse when a patent owner attempts to use the patent to exclude competitors from their marketplace knowing that the patent was invalid or unenforceable.
A patent will not be rendered unenforceable for misuse if the patent owner has enforced the patent in the good faith belief that the accused products infringed the patent’s claims.
You may consider all aspects of the conduct of the patent owner in deciding whether a patent has been misused. In order to find misuse, you may not determine that — you need not determine that an antitrust violation has been proved. Even if an antitrust violation has not been proven, you may still find that the patents have been misused if you conclude that the patents have been used wrongfully.
This instruction calls to mind the view expressed in USM Corp. v. SPS Techs., Inc.,
M3 Systems did not propose any of the classic grounds of patent misuse, such as tying or enforced package licensing or price restraints or extended royalty terms, see Chisum, supra, § 19.04[3], but generally urged the view that Bard’s actions, even if not illegal, were an improper use of patents. Although the law should not condone wrongful commercial activity, the body of misuse law and precedent need not be enlarged into an open-ended pitfall for patent-supported commerce.
There was no evidence that Bard’s competitive activities were either per se patent misuse or that they were not “reasonably within the patent grant.” See Mallinckrodt,
The verdicts of patent misuse are not supported by evidence or correct legal theory. The judgment on these verdicts is reversed.
Other Arguments/Issues
We have not discussed every minor argument and issue raised in this appeal. All have been considered, and we have discussed those of relevance. With respect to Bard’s frequent references to jury prejudice resulting from disclosure to the jury of Bard’s recent civil penalties and criminal convictions for several violations of Food and Drug Administration laws and regulations, we take
Costs
No costs.
AFFIRMED IN PART, REVERSED IN PART, VACATED IN PART, AND REMANDED
Notes
. C.R. Bard, Inc. v. M3 Sys., Inc., No. 93-CV-4788 (N.D. Ill. Oct. 2 & Dec. 20, 1995) (orders).
. § 102. A person shall be entitled to a patent unless—
(a) the invention was known or used by others in this country, or patented or described in a printed publication in this or a foreign country, before the invention thereof by the applicant for patent, ...
. § 102 A person shall be entitled to a patent unless—
(b) the invention was patented or described in a printed publication in this or a foreign country or in public use or on sale in this country, more than one year prior to the date of the application for patent in the United States, ....
. This section is the dissenting opinion of Judge Newman. The court affirms the judgment of invalidity for violation of the on-sale bar, in separate opinions of Chief Judge Mayer and Judge Bryson.
. The three different views in the three opinions of this panel on the on-sale issue point up the need for a more certain law than today exists. Inventors and those who commercialize inventions should reasonably know when the on-sale bar starts to accrue, instead of awaiting litigation-borne post hoc judicial evaluations of the totality of the circumstances, varying with the nature of the invention, the nature of the customer contact, and the judicial weight given to the conflicting policy interests.
I favor, as simple and fair, the bright line rule that for the § 102(b) on-sale bar to accrue the invention must exist in commercial form when the offer of sale is made. This rule would implement the dominant policy of providing a one-year grace period for determining the performance of the product in the marketplace.
. The record provided us does not show any response from the PTO. Although Bard states that "the [PTO] determined that the transfers to American Pharmaseal [] were for primarily experimental purposes and therefore did not trigger the bar,” the record citations do not relate to this statement.
. In Nobelpharma the Federal Circuit held in banc that Federal Circuit law would thenceforth apply to determination of whether fraudulent conduct occurred in obtaining a patent, whereas determination of the other elements of the section 2 violation, viz. market power in the relevant market and illegal restraints on competition, since not unique to the patent right would continue to be governed by regional circuit law.
. M3 in its brief states that: "The Jury specifically found that BARD had ‘actual knowledge' that M3 did not infringe its patents or that the patents were invalid. [A10096; 11-3 ¶¶ 6,11].” There is no specific finding in the verdict form of "actual knowledge.” The cites to ¶¶ 6 & 11 are to the jury's finding of patent misuse, and the jury instructions at A10096 concern the duty of candor to the PTO. The source of the quoted "actual knowledge” is not given. Such misdirections are not helpful to the appellate tribunal; see also note 6, supra.
. The court has affirmed the district court’s judgment of antitrust violation on this ground; see the separate opinion of Judge Biyson, joined by Chief Judge Mayer. This section contains the dissenting opinion of Judge Newman.
Concurrence Opinion
eoncurring-in-part and dissenting-in-part.
I join the court’s opinion as it pertains to the validity and infringement of the ’308 patent, and agree that the jury’s verdict on fraud cannot stand. I join Judge Bryson’s opinion sustaining the jury verdict on M3’s antitrust counterclaim and remanding. My views on the validity of the ’056 patent follow.
By special interrogatory, a jury found each of the disputed claims of the ’056 patent invalid because the claimed invention was on sale in the United States more than one year before July 30, 1986, the filing date of the ’056 patent’s parent application. M3 Systems presented the jury with two reasons why the invention may be invalid for violation of the on sale bar: a transfer from Radiplast to Pharmaseal of 250 needles in June 1985 and an offer from Radiplast to Dr. Ronald Phelps in November 1984. We may affirm the invalidity verdict on either basis. See, e.g., Ethicon Endo-Surgery, Inc. v. United States Surgical Corp.,
Discussion
An inventor who places his invention “in public use or on sale in this country, more than one year prior to the date of the application for patent in the United States” loses his right to patent the invention. 35 U.S.C. § 102(b) (1994). A determination that a product was placed on sale under section 102(b) is a question of law, based on underlying facts. See, e.g., KeyStone Retaining Wall Sys. Inc. v. Westrock, Inc.,
We are guided in our review of the legal conclusion by principles underlying the on sale bar: broad and prompt disclosure of inventions to the public; providing opportunity to experiment, improve, and determine the market value of inventions; discouraging inventors from withdrawing inventions that the public has already come to believe are freely available; and discouraging commercialization that expands the patent system’s grant of the right to exclude others. See, e.g. Envirotech Corp. v. Westech Eng’g, Inc.,
We are likewise guided in our review by the principle that we must presume facts necessary to support the jury verdict. See, e.g., Perkin-Elmer,
I. Offer for Sale
On September 25, 1984, Ronald Phelps, an Alabama medical doctor, sent Radiplast AB a letter that stated: “I am interested in learning more about the new device for percutaneous needle biopsy pictured on the enclosed brochure. I would appreciate it if you would send me all the information you have pertaining to the instrument. Also, please include a price list. Thank you.” Phelps included with this letter a brochure entitled “Radi-biospy device, a new device for percutaneous needle biopsy.” This brochure described previously existing technology and then stated:
A new device has been constructed in order to improve this biopsy method. With the aid of this instrument the biopsy procedure can be carried out with one hand, and as the movements of the obturator and cannula are automatized, better tissue specimens are obtained. All biopsies can be performed by one examiner under dynamic ultrasonic control, or under fi[uo]roscopy.
The new device consists of a spring-trigger system for firing the two different parts of the needle — the cannula and the obturator.
It is constructed of alloyed brass and, like the pressure rod, can be autoclaved.
See special instructions before using.
Manufactured by ... RADIPLAST AB....
By way of its managing director, Thomas Engstrom, Radiplast, replied as follows to Phelps’ letter on November 12,1984:
We thank you for your letter of [S]ept. 25[,] 1984 and for your interest in our BIOPSY DEVICE. I am truly sorry for my late reply.
Our generation No. 2 of the device will we, together with our new biopsy needles suitable for the device, start marketing in USA beginning of — 85, at the moment we do not know through which company.
If you do not want to wait until we have our representation in USA arranged, you can always [sic] order the device directly from us.
Our price for the device is SEK 9.900,- and for the needles SEK 75/ea.
The device is reusable and can be auto-claved. Very little service has to be done on the device due to reliable design. The needles are disposable and are designed to suit the device.
I am enclosing leaflet and article.
*1376 I am looking forward to hearing from you.
(Emphasis added).
The Radiplast brochure that Phelps sent to Radiplast describes a device that can be operated with one hand, by one operator, leaving the physician’s other hand free to operate the ultrasound or fluoroscopy equipment. The brochure, describes both parts of the needle as automatized by way of a spring-trigger system. It describes the construction materials used to manufacture the device as well as a procedure by which it can be cleaned. In short, the brochure can be understood to describe either a first generation prior art device or the second generation device described in the ’056 patent.
Despite this ambiguity, Engstrom’s reply to Phelps’ letter in November 1984 is far more telling both in what it said and when it said it. His letter explicitly refers to the second generation device and “new biopsy needles suitable for the device.” Since the second generation device requires a needle that moves both forward and rearward, unlike the prior art TruCut needle, Engstrom’s letter is a clear offer for sale of the second generation device and new biopsy needles. With the exception of a reference to marketing efforts being made in the United States and the possibility of sales through a United States distributor thereafter, this letter was written entirely in the present tense.
The letter was also written after a series of correspondence between Radiplast and Hart Enterprises, a United States medical device manufacturer, addressing tooling and manufacturing costs for these new biopsy needles. On September 4, 1984, Engstróm had written: “Enclosed please find ... a drawing on the biopsy needle. The stainless steel parts are not the final ones, there could be changes in length, diam. and the design of the point.” On September 28, 1984, Hart Enterprises responded: “[Ejnclosed are two drawings, one of the Stylet Hub and one of the Cannula Hub for your Radiplast Biopsy Needle. If you approve these concepts we will proceed to make a prototype, and then production of the molds.” Radiplast replied on October 18, 1984: “Biopsy needles: Enclosed please find our order for tooling and engineering. We approve your design of the plastic parts. The dimension from the top surface to center line of both cannula and stylet should be 4.2 mm. Regarding the needles we will probably start with 2.000 — 3.000 units bulk packed.” Less than one month later, Eng-stróm sent Phelps the November 12, 1984, letter.
These facts alone are sufficient support for the jury’s verdict that there was a definite offer for sale of something more than the TruCut prior art or first generation needles. However, to apply the on sale bar, the jury also had to decide whether this offer for sale of new biopsy needles was an offer of the invention claimed in the ’056 patent. We review this second presumed factual finding for substantial evidence, and like the district court on its denial of Bard’s motion for judgment as a matter of law, we also consider whether there may be policy considerations against imposing the on sale bar.
II. Offer of the Claimed Invention
Bard claims that Radiplast’s November 1984 offer to sell second generation devices and new biopsy needles cannot trigger the bar because at that time no operable device had been made, FDA approval had not been obtained, Radiplast had not conducted clinical testing, it had not found a United States distributor, and it had not developed a final needle design. Bard misapprehends the legal significance of each of these. Clinical testing is not required before a sale can bar patent rights. Nor can subsequent clinical testing excuse a prior sale, if what was offered for sale was the claimed invention. Clinical testing is merely one possible policy reason why a particular sale might be excused from the bar. Since Radiplast did not contemplate sales to Engstróm for testing purposes, the possibility of subsequent clinical testing is of no moment. Likewise, FDA approval is not required before a sale can bar patent rights. Even an illegal sale of the claimed invention before the critical date can bar patent rights. Nor is a domestic distrib
The first of Bard’s two remaining arguments — that no operable device had been made — is a feint because manufacture of an operable device is not a prerequisite for application of the on sale bar. See, e.g., Barmag Barmer Maschinenfabrik AG v. Murar ta Machinery, Ltd.,
As support for its remaining contention— that it had not developed the final design of the biopsy needle — Bard points to Eng-strom’s testimony, as managing director of Radiplast, and correspondence between Ra-diplast, American Pharmaseal, (one of Radi-plast’s potential distributors in the United States), and Alan Taylor (president of Hart Enterprises). Each of these letters was sent after the November 1984 offer for sale to Phelps, and each evidences continued testing of and proposed modifications to the second generation device and the new biopsy needles.
Engstrom testified that American Pharma-seal’s research and development laboratories conducted in-house testing. A technical report produced after this testing says that “testing [was] to insure functionality of the spring loaded activatior, the Biopty™ device, and the needle before releasing them to the field trial.” As a result of its testing, American Pharmaseal recommended: “increasing] the strength of the stylet handle design and adding] the buffing operation to cannula grinding process.” Engstrom testified that this advice was “to, how do you say, make some changes on the plastic parts and also the— what do you call that— well, the, for some plastic parts broke actually, so we put some, a stopper in the second generation device to prevent, if that happened, to prevent the stylet to go further on.” Engstrom testified that on American Pharmaseal’s advice, Radiplast added a “stop” to the second generation device, after the offer to Phelps.
Engstrom also testified that Radiplast conducted field trials in December 1985, from which it learned that “there was a potential risk for this one snapping back and hurt the doctor’s hand,” and “many patients thought the noise of the instrument was very disturbing.” As a result, Radiplast added “an automatic retraction, a spring, actually, which took this handle back,” and “some damping things, you know, to reduce the noise of the instrument.” After these field trials, Eng-strom sent a letter to Hart Enterprises on
This evidence suggests that Radiplast modified the second generation device by altering the strength of the stylet handle design, adding a buffing operation to the cannula grinding process, a stopper, automatic retraction via a spring, damping to reduce noise, and equal length symmetrical cannula hub wings as long as the shortest wing. However, Bard cannot avoid the on sale bar merely by showing improvements to the invention after its commercialization. See, e.g., Seal-Flex, Inc. v. Athletic Track and Court Constr.,
Because Bard’s evidence shows nothing beyond unclaimed mechanical adjustments to the needle design claimed in the ’056 patent after the November 1984 offer for sale of new biopsy needles, the jury had substantial evidence in support of its finding that the November 1984 offer for sale generated a statutory bar. See, e.g., Robotic Vision Sys., Inc. v. View Eng’g, Inc.,
III. Policy Considerations
Other than the need for sufficient time to test the new biopsy needle design, which is not a policy consideration summoned by the November 1984 offer, Bard has not argued that there are policy considerations weighing against imposition of the on sale bar. Since the policies that underlie the bar focus on the inventors attempts to exploit the invention, not whether a potential purchaser was made aware of or understood it, discussion of Phelps’ actual knowledge of the details of the invention or the differences between generations of the biopsy gun is irrelevant. See, e.g., Ferag,
Reliance on Engstrom’s trial testimony is inherently less reliable than contemporaneous documentary evidence. Cf. TP Lab., Inc. v. Professional Positioners, Inc.,
Concurrence Opinion
concurring in part and dissenting in part.
I concur in the portion of the court’s opinion upholding the jury’s verdict of non-in
With respect to portions of the judgment relating to the ’056 patent, I agree with Chief Judge Mayer that the ’056 patent is invalid under the “on-sale bar” of 35 U.S.C. § 102(b), although I take a somewhat different analytical path to that conclusion, as discussed below. Because I conclude that the ’056 patent is invalid based on the on-sale bar, I do not reach the other grounds on which the jury found the ’056 patent invalid.
Finally, Chief Judge Mayer and I agree that the jury verdict on M3’s antitrust counterclaim must be affirmed. Because we do not uphold all of the grounds on which the jury found liability, however, we conclude that the jury may have improperly assessed damages on liability grounds that cannot stand. We therefore must remand for further proceedings to determine the proper amount of damages to be assessed on the antitrust counterclaim.
I
With respect to the on-sale bar, I believe that the June 1985 sale of 250 needles from Radiplast to Pharmaseal was sufficient to support the jury’s verdict that the asserted claims of the ’056 patent were rendered invalid by a sale more than one year before July 30, 1986, the effective filing date of the patent. It is undisputed that the needles sold in June 1985 embodied the invention of the ’056 patent. Whether that sale was sufficient to invoke the on-sale bar turns on whether the sale falls within the “experimental purpose” exception to the on-sale bar.
A
In the summer of 1984, Radiplast began looking for a company “to distribute and promote the sales of [its] biopsy instruments in the United States.” Pharmaseal, a potential distributor of the instruments, sent a telex to Radiplast stating that “before any formal purchasing plans can be made,” it would have to conduct field trials “to determine the performance and specimen quality of your biopsy device and disposable needle.” Pharmaseal sent letters to several hospitals in December 1984 inviting them to participate in a “field trial as a potential sales/distribution system for Radiplast devices.”
Radiplast responded by telex on January 21, 1985, setting a price for the needles to be used in Pharmaseal’s field trial and offering large-quantity discounts for batches of up to 50,000 needles. Radiplast’s telex stated that “in order to be able to deliver both needles and instruments in beginning of March [1985], we need a [telex] order, preferably this week.” It also stated that “we have to meet and discuss more in detail all things related with the marketing of our biopsy instrument in U.S.” With respect to Pharma-seal’s proposed field trial, Radiplast merely suggested that “if you would like [Dr. Lind-gren, the inventor] to visit the hospitals performing the trial, in order to help them get started, he will be happy to help you.”
Pharmaseal agreed to purchase the instruments and, on March 28, 1985, placed an order for 10 biopsy guns and 250 needles from Radiplast. The instruments were shipped in June 1985. It is undisputed that the June 1985 transaction constituted a sale and that the needles sold at that time embodied the invention of the ’056 patent.
Pharmaseal conducted in-house testing of the devices in July 1985 before releasing the products to hospitals for the field trials. Following the in-house testing, Pharmaseal reported only minor problems and made minor manufacturing suggestions, such as recommending that Radiplast strengthen the stylet hub design and add a buffing operation to the cannula grinding process.
Although Bard contends that Dr. Lindgren attended some of the field trials and that Radiplast “was continually advised by Phar-maseal of [their] progress,” Dr. Lindgren
The field testing was performed at the behest of Pharmaseal, the purchaser, not Ra-diplast or the inventor. Pharmaseal “assumed primary responsibility” for the tests, while Radiplast merely “had an ongoing interest” in the progress of the trials and “was kept informed” of the progress of the field trials. During the field trials, Pharmaseal and Radiplast continued to discuss market potential, potential prices and volumes, and an instructional videotape to teach proper use of the instruments.
B
Bard argues that the jury verdict cannot stand because the in-house testing at Phar-maseal and the hospital field trials show that the sale was for experimental testing purposes. The so-called “experimental testing” exception to the on-sale bar applies only if commercial exploitation is “merely incidental to the primary purpose of experimentation to perfect the invention.” Barmag Barmer Maschinenfabrik AG v. Murata Mach., Ltd.,
The evidence shows that Radiplast’s primary purpose in making the sale to Pharma-seal was to market the patented invention through Pharmaseal, not to conduct tests to determine whether the claimed invention would work for its intended purpose. Neither the in-house testing at Pharmaseal nor the field trials at hospitals were conducted under the control or supervision of the inventor or Radiplast; instead, the tests were proposed, controlled, and monitored by Phar-maseal, the purchaser. Dr. Lindgren, the inventor, admitted at trial that he had no control over the field trials, that he did not maintain any test data, and that he did not recall receiving any test results. Radiplast was not aware of the identity of the patients in the field tests, the organs that were being biopsied, or the types of tests being performed; indeed, the patients were apparently not even informed that the biopsies were being conducted as part of a test. The hospitals participating in the field trials were told that the trials were intended as “a potential sales/distribution system for Radiplast devices.” There is no evidence that any secrecy agreements were made with Pharmaseal, the hospitals, or any of the test participants. Finally, it is undisputed that Pharmaseal paid for the instruments and needles used in the tests. All of these factors point away from the conclusion that the sale was made for purposes of experimentation. See Western Marine Elecs., Inc. v. Furuno Elec. Co.,
The facts of this case are analogous to those in U.S. Environmental Products, Inc. v. Westall,
Bard relies heavily on Continental Can Co. USA, Inc. v. Monsanto Co.,
C
Bard also contends that the Pharmaseal sale cannot constitute a bar under 35 U.S.C. § 102(b) because Radiplast did not make a profit on the transaction. The jury heard testimony, however, suggesting that Radi-plast made a 60% profit on the Pharmaseal sale. Even ignoring any actual profit on the devices used in the field trials, it is clear that the Pharmaseal transaction was made primarily to develop a market for future sales, not primarily to test the claimed invention. At any rate, the failure to turn a profit is not determinative. “A patent owner may have created an on-sale bar despite losing money on a sale.” U.S. Envtl. Prods., Inc. v. Westall,
II
In support of its antitrust counterclaim, M3 presented three theories to the jury: (1)
A
The jury considered evidence that Bard modified its Biopty gun to prevent its competitors’ non-infringing, flangeless needles from being used in Bard’s guns. By special verdicts, the jury found that there was a relevant product market for replacement needles for fully automated reusable biopsy guns, that Bard had monopoly power in that market, and that it had acquired or maintained its monopoly power in that market through restrictive or exclusionary conduct.
In order to prevail on its claim of an antitrust violation based on Bard’s modification of its Biopty gun to prevent the use of competing replacement needles, M3 was required to prove that Bard made a change in its Biopty gun for predatory reasons, ie., for the purpose of injuring competitors in the replacement needle market, rather than for improving the operation of the gun. See In re IBM Peripheral EDP Devices Antitrust Litig.,
The dissent on this issue starts from the premise that the modification to Bard’s Biopty gun was an “improvement” and argues from that premise that to hold Bard liable for the modification would have the “pernicious” effect of penalizing innovators for making improvements to their products. The dissent’s premise, however, is contrary to the jury’s verdict, which was supported by the evidence. Although Bard contended at trial that it modified its Biopty gun to make it easier to load and unload, there was substantial evidence that Bard’s real reasons for modifying the gun were to raise the cost of entry to potential makers of replacement needles, to make doctors apprehensive about using non-Bard needles, and to preclude the use of “copycat” needles. One internal Bard document showed that the gun modifications had no effect on gun or needle performance; another internal document showed that the use of non-Bard needles in the gun “could not possibly result in injury to either the patient or the physician.” In view of that evidence, the jury could reasonably conclude that Bard’s modifications to its guns constituted “restrictive or exclusionary conduct” in a market over which it had monopoly power.
The dissent also takes issue with the jury instructions, contending that they failed properly to frame a charge of predatory conduct that comports with established criteria of antitrust liability. Because Bard did not challenge the court’s instructions, however, the legal sufficiency of the jury charge on the antitrust issues is not properly before us on appeal. To be entitled to relief based on asserted errors in the court’s instructions to
B
While we affirm Bard’s liability on the antitrust counterclaim, that does not necessarily mean that the jury’s damage award of $1.5 million can be sustained. M3 presented evidence of three different markets (guns, guns and needles, and replacement needles) in which Bard allegedly caused antitrust injury, and the jury found Bard liable for injury in each market. The damages portion of the verdict, however, merely indicated a general award of $1.5 million without attribution to a particular market or exclusionary practice.
M3’s evidence concerning Bard’s gun modification program was relevant only to the replacement needle market. Because we have concluded that the evidence concerning Bard’s activities in the other two markets cannot support antitrust liability, the question arises as to whether the $1.5 million damages award can be supported solely on the basis of the injury Bard’s actions caused to M3 in the replacement needle market. That issue was not briefed on appeal, and the record, so far as we can ascertain, does not provide clear guidance as to the proper allocation of damages due to the injury suffered by M3 in-the injury replacement needle market. Consequently, wé vacate the antitrust damages award and remand to the district court to consider, after additional hearing or limited retrial, if necessary, the proper amount of damages attributable to Bard’s gun modification program. See MCI Communications Corp. v. American Tel. & Tel. Co.,