K-number	K903243
Device name	MULLER-TYPE FEMORAL COMPONENT
Applicant	Onyx Medical Corp.
Product code	JDI
Device class	Class II
Decision date	Jul 30, 1990
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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MULLER-TYPE FEMORAL COMPONENT

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