K-number	K032295
Device name	GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT
Applicant	Smith & Nephew, Inc.
Product code	JWH
Device class	Class II
Decision date	Aug 21, 2003
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT

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