K-number	K063822
Device name	MODIFICATION TO HIPSTAR FEMORAL STEM
Applicant	Stryker Orthopaedics
Product code	LPH
Device class	Class II
Decision date	Jan 25, 2007
Decision	Substantially Equivalent
Regulation	888.3358

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO HIPSTAR FEMORAL STEM

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