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M-Vizion Femoral Revision System Extension

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191816
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/29/2020
Days to Decision
299 days
Submission Type
Summary

M-Vizion Femoral Revision System Extension

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191816
510(k) Type
Traditional
Applicant
Medacta International SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/29/2020
Days to Decision
299 days
Submission Type
Summary