Junker v. Medical Components, Inc.

CourtCourt of Appeals for the Federal Circuit
DecidedFebruary 10, 2022
Docket21-1649
StatusPublished

This text of Junker v. Medical Components, Inc. (Junker v. Medical Components, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Junker v. Medical Components, Inc., (Fed. Cir. 2022).

Opinion

Case: 21-1649 Document: 53 Page: 1 Filed: 02/10/2022

United States Court of Appeals for the Federal Circuit ______________________

LARRY G. JUNKER, Plaintiff-Appellee

v.

MEDICAL COMPONENTS, INC., MARTECH MEDICAL PRODUCTS, INC., Defendants-Appellants ______________________

2021-1649 ______________________

Appeal from the United States District Court for the Eastern District of Pennsylvania in No. 2:13-cv-04606- MSG, Judge Mitchell S. Goldberg. ______________________

Decided: February 10, 2022 ______________________

JAMES D. PETRUZZI, The Petruzzi Law Firm, Houston, TX, argued for plaintiff-appellee. Also represented by LAURA MAUPIN, Maupin Redman, Livingston, TX.

ALFRED W. ZAHER, I, Montgomery McCracken Walker & Rhoads LLP, Philadelphia, PA, argued for defendants- appellants. Also represented by JOSEPH MONAHAN. ______________________

Before DYK, REYNA, and STOLL, Circuit Judges. Case: 21-1649 Document: 53 Page: 2 Filed: 02/10/2022

STOLL, Circuit Judge. Larry G. Junker, the named inventor of U.S. Design Patent No. D450,839, sued Medical Components, Inc. and Martech Medical Products, Inc. (collectively, “MedComp”) for infringement of the sole claim of the D’839 patent. The parties filed cross-motions for summary judgment, debat- ing whether a letter sent before the critical date was a com- mercial offer for sale of the claimed design, rendering the claim invalid under the on-sale bar, 35 U.S.C. § 102(b). The district court granted Mr. Junker’s motion for sum- mary judgment of no invalidity under the on-sale bar. The district court thereafter held a bench trial on several re- maining issues in the case, including MedComp’s remain- ing invalidity challenges, infringement, and damages. The court again ruled in Mr. Junker’s favor. The court rejected each of MedComp’s invalidity challenges, found that each of the accused products infringed the D’839 patent claim and that the infringement was willful, and awarded Mr. Junker $1,247,910 in damages under 35 U.S.C. § 289, which allows recovery of an infringer’s profits from sale of the infringing products. MedComp appeals the district court’s summary judg- ment of no invalidity under the on-sale bar, the judgment of infringement, and the damages award. For the reasons below, we agree with MedComp that the pre-critical date letter was a commercial offer for sale. Because there is no dispute that the claimed design was ready for patenting, we reverse the district court’s summary judgment of no in- validity. We therefore do not reach the remaining issues on appeal. Case: 21-1649 Document: 53 Page: 3 Filed: 02/10/2022

JUNKER v. MEDICAL COMPONENTS, INC. 3

BACKGROUND I The D’839 patent, at the heart of the dispute on appeal, is titled “Handle for Introducer Sheath,” and includes a sin- gle claim for “[t]he ornamental design for a handle for in- troducer sheath, as shown and described.” D’839 patent, claim. Figure 1 shows a perspective view of the claimed design (represented with solid lines):

Id. Fig. 1. Mr. Junker filed the application that led to the D’839 patent on February 7, 2000. Thus, the critical date for analyzing the on-sale bar under § 102(b) 1 is February 7, 1999, one year before the filing date.

1 Congress amended § 102 when it enacted the Leahy–Smith America Invents Act (AIA). Pub. L. No. 112–29, § 3(b)(1), 125 Stat. 284, 285–87 (2011). How- ever, because the application that led to the D’839 patent Case: 21-1649 Document: 53 Page: 4 Filed: 02/10/2022

A Mr. Junker started working in the medical device in- dustry in the 1970s. In the late 1970s, Mr. Junker started his own company for purchasing and reselling catheter kits. These kits typically included a needle, syringe, guide- wire, and introducer sheath that were used for inserting a catheter into the vein of a patient. Mr. Junker’s company also designed and manufactured some components in the kits, including the introducer sheath. In the mid-1980s, Mr. Junker began developing a new design for the intro- ducer sheath based on his experience observing catheter- insertion procedures. Mr. Junker focused on the design for the introducer sheath’s handle, eventually settling on a handle with large, rounded Mickey-Mouse-shaped ears that made it easier for doctors to grasp the introducer sheath during catheter-insertion procedures. The handle was designed such that the sheath could be peeled apart into two pieces when removing the sheath while leaving the catheter in place in the patient’s body. These products are referred to as “peelable,” “peel-away,” or “tearaway” in- troducer sheaths. Mr. Junker, however, did not have the proper machin- ery to manufacture the product. He began reaching out to other companies to handle the actual manufacture of his new design. Eventually, in 1998, Mr. Junker developed a business relationship with James Eddings, the founder of a medical device company called Galt Medical. At their first meeting in August 1998, Mr. Junker and Mr. Eddings entered into a non-disclosure agreement (Mr. Junker on behalf of his company and Mr. Eddings on behalf of Galt), after which Mr. Junker told Mr. Eddings about his new de- sign for the introducer sheath handle. The next month, in September 1998, Mr. Eddings informed Mr. Junker that

was filed before March 16, 2013, the pre-AIA § 102 applies. See id. § 3(n)(1), 125 Stat. at 293. Case: 21-1649 Document: 53 Page: 5 Filed: 02/10/2022

JUNKER v. MEDICAL COMPONENTS, INC. 5

Galt could manufacture Mr. Junker’s product. Around this same time, Mr. Eddings also founded a new company, Xentek Medical, to develop, manufacture, and sell teara- way introducer sheath products. Over the course of the next several months, Mr. Junker and Mr. Eddings continued to discuss Mr. Junker’s new de- sign. Mr. Eddings enlisted the help of an engineer, Richard Gillespie, to sketch out Mr. Junker’s proposed design. Af- ter some back and forth, Mr. Gillespie provided Mr. Junker with a sketch of the design. This sketch, however, was lacking the handles with Mickey Mouse ears that Mr. Jun- ker had envisioned. In a fax dated December 16, 1998, Mr. Junker relayed his critiques of the sketch to Mr. Ed- dings, noting the absence of larger, rounded portions on the handle and providing a rough sketch of his design as he had imagined it. Mr. Eddings asked Mr. Gillespie to mod- ify the sketch accordingly. In January 1999, Mr. Eddings’ company, Xentek, developed and provided to Mr. Junker a prototype of the product that included all of the features of his design, including (importantly) a handle with Mickey Mouse ears. B In early January 1999, Mr. Eddings, through Xentek, began communicating with Boston Scientific Corporation regarding a peelable introducer sheath product. In re- sponse to a request from Boston Scientific, on January 8, 1999, Xentek sent Boston Scientific a letter detailing bulk pricing information for variously sized peelable introducer sheath products. The letter stated: Thank you for the opportunity to provide this quo- tation for the Medi-Tech Peelable Sheath Set. When we first received this request for quotation we were under the mistaken impression that you wanted the exact configuration as the drawing that was provided which would have required extensive tooling expense. Subsequently, we have learned Case: 21-1649 Document: 53 Page: 6 Filed: 02/10/2022

that this is not the case and are pleased to submit this quotation for a product of our design. ... The principals of Xentek Medical have extensive experience in the design, development and manu- facture of this type of medical device.

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