K-number	K070883
Device name	DURACON X3 CS TIBIAL INSERT
Applicant	Howmedica Osteonics Corp.
Product code	MBH
Device class	Class II
Decision date	May 11, 2007
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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DURACON X3 CS TIBIAL INSERT

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