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M-Vizion Femoral Revision System

Page Type
Cleared 510(K)
510(k) Number
K170690
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/29/2017
Days to Decision
267 days
Submission Type
Summary

M-Vizion Femoral Revision System

Page Type
Cleared 510(K)
510(k) Number
K170690
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/29/2017
Days to Decision
267 days
Submission Type
Summary