K-number	K031730
Device name	36MM ORTHINOX V40 FEMORAL HEAD COMPONENTS
Applicant	Howmedica Osteonics Corp.
Product code	JDI
Device class	Class II
Decision date	Aug 29, 2003
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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36MM ORTHINOX V40 FEMORAL HEAD COMPONENTS

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