K-number	K090757
Device name	BIOMET MODULAR FEMORAL REVISION SYSTEM
Applicant	Biomet, Inc.
Product code	KWA
Device class	Class III
Decision date	Sep 25, 2009
Decision	Substantially Equivalent
Regulation	888.3330

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View the full FDA submission: accessdata.fda.gov

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BIOMET MODULAR FEMORAL REVISION SYSTEM

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