K-number	K910093
Device name	FUTURA FEMORAL HIP STEM
Applicant	O'Tec Corp.
Product code	JDI
Device class	Class II
Decision date	Jul 1, 1991
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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FUTURA FEMORAL HIP STEM

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