K-number	K001374
Device name	PATIENT MATCHED COBALT ALLOY TROCHLEA REPLACEMENT
Applicant	Biomet Manufacturing, Inc.
Product code	KRR
Device class	Class II
Decision date	Jul 27, 2000
Decision	Substantially Equivalent
Regulation	888.3540

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View the full FDA submission: accessdata.fda.gov

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PATIENT MATCHED COBALT ALLOY TROCHLEA REPLACEMENT

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