K-number	K911052
Device name	NEXUS(TM) FEMORAL HIP STEM
Applicant	Dow Corning Wright
Product code	JDI
Device class	Class II
Decision date	Jun 17, 1991
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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NEXUS(TM) FEMORAL HIP STEM

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