K-number	K103170
Device name	GMK REVISION KNEE SC LINERS
Applicant	Medacta International S.A.
Product code	JWH
Device class	Class II
Decision date	Mar 24, 2011
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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GMK REVISION KNEE SC LINERS

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