K-number	K830750
Device name	CEMENTED 101 32 FEMORAL COMPONENT
Applicant	Intermedics Orthopedics
Product code	JDI
Device class	Class II
Decision date	May 2, 1983
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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CEMENTED 101 32 FEMORAL COMPONENT

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