K-number	K072336
Device name	REGENEREX POROUS TITANIUM SLEEVE AUGMENTS
Applicant	Biomet Manufacturing Corp
Product code	JWH
Device class	Class II
Decision date	Nov 5, 2007
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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REGENEREX POROUS TITANIUM SLEEVE AUGMENTS

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