K-number	K010664
Device name	COPELAND RESURFACING HUMERAL HEADS
Applicant	Biomet Manufacturing, Inc.
Product code	HSD
Device class	Class II
Decision date	Apr 5, 2001
Decision	Substantially Equivalent
Regulation	888.3690

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View the full FDA submission: accessdata.fda.gov

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COPELAND RESURFACING HUMERAL HEADS

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