K-number	K163311
Device name	GMK Revision Femoral Distal Augmentation
Applicant	Medacta International S.A.
Product code	KRO
Device class	Class II
Decision date	Dec 21, 2016
Decision	Substantially Equivalent
Regulation	888.3510

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Source

View the full FDA submission: accessdata.fda.gov

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GMK Revision Femoral Distal Augmentation

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