K-number	K990183
Device name	IMPLEX ALUMINA FEMORAL HEAD
Applicant	Implex Corp.
Product code	LZO
Device class	Class II
Decision date	Jun 11, 1999
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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IMPLEX ALUMINA FEMORAL HEAD

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