K-number	K031804
Device name	COMPRESS DISTAL FEMORAL REPLACEMENT
Applicant	Biomet, Inc.
Product code	KRO
Device class	Class II
Decision date	Dec 18, 2003
Decision	Substantially Equivalent
Regulation	888.3510

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View the full FDA submission: accessdata.fda.gov

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COMPRESS DISTAL FEMORAL REPLACEMENT

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