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GMK Revision Femoral Distal Augmentation

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163311
510(k) Type
Special
Applicant
Medacta International S.A.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163311
510(k) Type
Special
Applicant
Medacta International S.A.
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/21/2016
Days to Decision
28 days
Submission Type
Summary