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Glenoid Reconstruction System – Full Wedge Baseplate

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231911
510(k) Type
Traditional
Applicant
Medacta International S.A.
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/9/2023
Days to Decision
133 days
Submission Type
Summary

Glenoid Reconstruction System – Full Wedge Baseplate

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231911
510(k) Type
Traditional
Applicant
Medacta International S.A.
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/9/2023
Days to Decision
133 days
Submission Type
Summary