K-number	K132435
Device name	SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS
Applicant	Smith & Nephew, Inc.
Product code	LZO
Device class	Class II
Decision date	Oct 22, 2013
Decision	Substantially Equivalent
Regulation	888.3353

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Source

View the full FDA submission: accessdata.fda.gov

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SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS

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