K-number	K925613
Device name	PROXIMAL HUMERAL REPLACEMENT SYSTEM
Applicant	Biomet, Inc.
Product code	KWT
Device class	Class II
Decision date	Oct 14, 1994
Decision	Substantially Equivalent
Regulation	888.3650

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View the full FDA submission: accessdata.fda.gov

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PROXIMAL HUMERAL REPLACEMENT SYSTEM

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