K-number	K012172
Device name	DURACON PS LIPPED TIBIAL INSERT
Applicant	Howmedica Osteonics
Product code	JWH
Device class	Class II
Decision date	Oct 10, 2001
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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DURACON PS LIPPED TIBIAL INSERT

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