K-number	K896853
Device name	PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA
Applicant	Howmedica Corp.
Product code	KWL
Device class	Class II
Decision date	May 2, 1990
Decision	Substantially Equivalent for Some Indications
Regulation	888.3360

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PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA

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