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GMK Revision Femoral Distal Augmentation

Page Type
Cleared 510(K)
510(k) Number
K163311
510(k) Type
Special
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/21/2016
Days to Decision
28 days
Submission Type
Summary

GMK Revision Femoral Distal Augmentation

Page Type
Cleared 510(K)
510(k) Number
K163311
510(k) Type
Special
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/21/2016
Days to Decision
28 days
Submission Type
Summary