K-number	K150241
Device name	Genesis II XLPE Resurfacing Patellar Components
Applicant	Smith & Nephew, Inc.
Product code	JWH
Device class	Class II
Decision date	Oct 27, 2015
Decision	Substantially Equivalent
Regulation	888.3560

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Source

View the full FDA submission: accessdata.fda.gov

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Genesis II XLPE Resurfacing Patellar Components

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