Last synced on 14 November 2025 at 11:06 pm

Glenoid Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K213459
510(k) Type
Traditional
Applicant
Medacta International S.A.
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/23/2022
Days to Decision
392 days
Submission Type
Summary

Glenoid Reconstruction System

Page Type
Cleared 510(K)
510(k) Number
K213459
510(k) Type
Traditional
Applicant
Medacta International S.A.
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
11/23/2022
Days to Decision
392 days
Submission Type
Summary