K-number	K971938
Device name	REPICCI II UNICONDYLAR KNEE
Applicant	Biomet, Inc.
Product code	HRY
Device class	Class II
Decision date	Aug 25, 1997
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

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