K-number	K001350
Device name	PATIENT MATCHED TITANIUM ALLOY TROCHLEA
Applicant	Biomet, Inc.
Product code	KRR
Device class	Class II
Decision date	Jul 26, 2000
Decision	Substantially Equivalent
Regulation	888.3540

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Source

View the full FDA submission: accessdata.fda.gov

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PATIENT MATCHED TITANIUM ALLOY TROCHLEA

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