K-number	K051086
Device name	SMITH & NEPHEW PATELLO-FEMORAL IMPLANT
Applicant	Smith & Nephew, Inc.
Product code	KRR
Device class	Class II
Decision date	May 31, 2005
Decision	Substantially Equivalent
Regulation	888.3540

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View the full FDA submission: accessdata.fda.gov

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SMITH & NEPHEW PATELLO-FEMORAL IMPLANT

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