K-number	K904737
Device name	GROSS HIP FEMORAL COMPONENT
Applicant	Johnson & Johnson Orthopaedics, Inc.
Product code	JDI
Device class	Class II
Decision date	Jul 26, 1991
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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GROSS HIP FEMORAL COMPONENT

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