K-number	K051223
Device name	HIPSTAR FEMORAL STEM
Applicant	Stryker Orthopaedics
Product code	LZO
Device class	Class II
Decision date	May 10, 2006
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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HIPSTAR FEMORAL STEM

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