Lenox MacLaren Surgical Corp. v. Medtronic, Inc.

847 F.3d 1221
CourtCourt of Appeals for the Tenth Circuit
DecidedFebruary 7, 2017
Docket15-1500 and 16-1012
StatusPublished
Cited by130 cases

This text of 847 F.3d 1221 (Lenox MacLaren Surgical Corp. v. Medtronic, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Tenth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Lenox MacLaren Surgical Corp. v. Medtronic, Inc., 847 F.3d 1221 (10th Cir. 2017).

Opinion

McHUGH, Circuit Judge.

I. INTRODUCTION

In 2010, Lenox MacLaren Surgical Corporation (“Lenox”) sued several related corporations — Medtronic, Inc.; Medtronic PS Medical, Inc. (“PS Medical”); Medtronic Sofamor Danek, Inc. (“MSD, Inc.”); and Medtronic Sofamor Danek Co. Ltd. (“MSD Japan”) (collectively, “Defendants”) — for monopolization and attempted monopolization in violation of § 2 of the Sherman Act. 15 U.S.C. § 2. Lenox alleged that Defendants engaged in illegal activity to advance a coordinated, anticompetitive scheme in which a related non-party, Medtronic Sofa-mor Danek USA, Inc. (“MSD USA”), also participated. Lenox had sued MSD USA in 2007 on claims arising from the same set of facts.

This appeal, the third in this case, challenges the district court’s disposition of Defendants’ second motion for summary judgment, which claimed that Lenox could not prove the elements of its antitrust claims against any of the named Defendants individually, and that Defendants cannot be charged collectively with the conduct of MSD USA or of each other. They also argued that the doctrine of claim preclusion bars Lenox’s claims, in light of the prior proceeding against MSD USA. The district court granted summary judgment, holding that because Lenox could not establish each of the elements of an antitrust claim against any one defendant, or establish a conspiracy among them, Le-nox’s claims fail as a matter of law.

Lenox now appeals, alleging several errors in the district court’s substantive analysis of Lenox’s § 2 claims. Defendants cross-appeal to preserve their argument that, even if the district court erred in resolving Lenox’s antitrust claims, we should affirm on the alternative basis of claim preclusion.

For the reasons set forth below, we conclude that Lenox raised a viable antitrust theory, but we decline to address the merits of Lenox’s antitrust claims because to the extent Defendants can be held liable under Lenox’s theory of antitrust liability, they are in privity with MSD USA. As a result, Lenox’s claims are barred by the claim preclusion arm of res judicata. We therefore affirm the district court’s grant of summary judgment for Defendants on that basis.

II. BACKGROUND

The parties’ dispute traces back to 2000, when Lenox entered into an agreement to sell bone mills — surgical tools that Lenox manufactures — through MSD USA. The arrangement with MSD USA did not go as Lenox had hoped: MSD USA initiated a recall of Lenox’s bone mills, and one of the present defendants, PS Medical, began to manufacture and sell its own bone mills to former users of Lenox’s product. As we explain in greater detail below, it is this failed arrangement that forms the factual nucleus of this case.

Before proceeding further into the background recitation, we pause to clarify the identities of, and relationships among, the several Medtronic entities involved in this dispute. In our decisions resolving the two prior appeals in this case, and in Lenox’s various filings in the district court, the four named defendants often are referenced as one: in Lenox MacLaren Surgi *1227 cal Corp. v. Medtronic, Inc. (Lenox I), 449 Fed.Appx. 704 (10th Cir. 2011) (unpublished), . they are “the Medtronic Defendants”; and in Lenox MacLaren Surgical Corp. v. Medtronic, Inc. (Lenox II), 762, F.3d 1114 (10th Cir. 2014), and many of Lenox’s filings, they are “Medtronic.” For purposes of assessing the district court’s order and the issues raised in this appeal, however, it is important to keep the actions of the various entities separate.

A. The Medtronic Entities

Medtronic, Inc. is the highest-tier Med-tronic entity named as a defendant in this case and is the parent or grandparent corporation of the other three defendants, as well as non-party MSD USA, the Med-tronic entity Lenox sued in the prior litigation and arbitration. PS Medical and MSD, Inc. are wholly owned subsidiaries of Med-tronic, Inc.; and MSD Japan and MSD USA are wholly owned subsidiaries of MSD, Inc. The relevant corporate structure thus looks like this:

• Medtronic, Inc. (defendant)
• MSD, Inc. (defendant)
• MSD Japan (defendant)
• MSD USA (non-party)
• PS Medical (defendant)

B. Factual History 1

Lenox was one of the first companies to design and produce a bone mill, which is a medical tool that grinds bone into fragments for use in spinal-fusion surgeries. In April 2000, Lenox entered into a five-year Exclusive Supply and License Agreement (the “license agreement” or the “agreement”) with MSD USA. The agreement granted MSD USA the exclusive right to purchase Lenox’s bone mills, rebrand them, and distribute them. In exchange, MSD USA promised to “refrain from purchasing [bone mills] from any third party or from producing [bone mills] itself,” and agreed to certain minimum purchase requirements. Specifically, the agreement required MSD USA to purchase 500 bone mills in the first year and to purchase 100 bone mills per quarter thereafter to maintain the exclusivity of. its distribution rights. Among other additional provisions, the agreement contained a dispute resolution clause under which the parties agreed to arbitrate “any dispute arising out of or relating to” the agreement.

MSD USA made the initial purchase of 500 bone mills in the first year but did not purchase any bone mills after that. Lenox therefore notified MSD USA in 2001 that its distribution rights were no longer exclusive.

MSD USA sold some of the 500 Lenox bone mills but distributed the rest through a “loaner program,” whereby doctors and hospitals could use the bone mills for free while MSD USA retained ownership of them. Under this program, the bone mills were returned to MSD USA after each surgery to be sterilized and redistributed for reuse. MSD USA sold or loaned some of the bone mills to MSD Japan, which marketed them to doctors and hospitals in Japan.

In November 2002, after MSD USA had purchased the 500 Lenox bone mills, PS Medical began developing a pneumatic bone mill of its own. This device proved commercially unsuccessful, and in 2006, PS Medical began developing a new electric bone mill called the Midas Rex.

Between 2000 and 2006, Lenox and MSD USA received only one complaint about Lenox’s bone mill — an April 2003 report from an MSD Japan representative stating that a piece of metal was found in *1228 the ground bone fragments produced by the device. Lenox reviewed the report, determined the malfunction was caused by user error, advised MSD USA of its determination, and did not hear anything further about the incident from MSD USA.

Then, on September 4, 2006, an MSD Japan representative generated three new complaints.

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Bluebook (online)
847 F.3d 1221, Counsel Stack Legal Research, https://law.counselstack.com/opinion/lenox-maclaren-surgical-corp-v-medtronic-inc-ca10-2017.