K-number	K020264
Device name	REPICCI II UNICONDYLAR KNEE SYSTEM
Applicant	Biomet Orthopedics, Inc.
Product code	HRY
Device class	Class II
Decision date	Feb 8, 2002
Decision	Substantially Equivalent
Regulation	888.3530

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View the full FDA submission: accessdata.fda.gov

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REPICCI II UNICONDYLAR KNEE SYSTEM

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