K-number	K062408
Device name	SMITH & NEPHEW MODULAR FEMORAL (HEMI) HEAD
Applicant	Smith & Nephew, Inc.
Product code	KWL
Device class	Class II
Decision date	Sep 12, 2006
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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SMITH & NEPHEW MODULAR FEMORAL (HEMI) HEAD

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