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M-Vizion Femoral Revision System Extension

Page Type
Cleared 510(K)
510(k) Number
K201471
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/11/2021
Days to Decision
222 days
Submission Type
Summary

M-Vizion Femoral Revision System Extension

Page Type
Cleared 510(K)
510(k) Number
K201471
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/11/2021
Days to Decision
222 days
Submission Type
Summary