K-number	K053003
Device name	DEPUY CMW 1, 2 AND 3 BONE CEMENTS
Applicant	DePuy Orthopaedics, Inc.
Product code	LOD
Device class	Class II
Decision date	Nov 22, 2005
Decision	Substantially Equivalent
Regulation	888.3027

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View the full FDA submission: accessdata.fda.gov

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DEPUY CMW 1, 2 AND 3 BONE CEMENTS

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