K-number	K992025
Device name	PRECISION OSTEOLOCK FEMORAL STEMS WITH PURE-FIX HA COATING
Applicant	Howmedica Osteonics Corp.
Product code	MEH
Device class	Class II
Decision date	Aug 13, 1999
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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PRECISION OSTEOLOCK FEMORAL STEMS WITH PURE-FIX HA COATING

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