K-number	K032683
Device name	GENESIS II POROUS PLUS HA KNEE SYSTEM
Applicant	Smith & Nephew, Inc.
Product code	MBH
Device class	Class II
Decision date	Oct 15, 2003
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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GENESIS II POROUS PLUS HA KNEE SYSTEM

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