K-number	K884837
Device name	KINEMAX TIBIAL WEDGE
Applicant	Howmedica Corp.
Product code	HRY
Device class	Class II
Decision date	Feb 17, 1989
Decision	Substantially Equivalent
Regulation	888.3530

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View the full FDA submission: accessdata.fda.gov

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KINEMAX TIBIAL WEDGE

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