K-number	K011138
Device name	OXFORD UNICOMPARTMENTAL KNEE FEMORAL COMPONENT
Applicant	Biomet, Inc.
Product code	HRY
Device class	Class II
Decision date	Jul 10, 2001
Decision	Substantially Equivalent
Regulation	888.3530

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View the full FDA submission: accessdata.fda.gov

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OXFORD UNICOMPARTMENTAL KNEE FEMORAL COMPONENT

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