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Univers Revers Modular Glenoid System, Standard Augment Baseplates

Page Type
Cleared 510(K)
510(k) Number
K211074
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2021
Days to Decision
143 days
Submission Type
Summary

Univers Revers Modular Glenoid System, Standard Augment Baseplates

Page Type
Cleared 510(K)
510(k) Number
K211074
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2021
Days to Decision
143 days
Submission Type
Summary