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Univers Revers Modular Glenoid System (Augemented baseplates)

Page Type
Cleared 510(K)
510(k) Number
K193372
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2020
Days to Decision
36 days
Submission Type
Summary

Univers Revers Modular Glenoid System (Augemented baseplates)

Page Type
Cleared 510(K)
510(k) Number
K193372
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2020
Days to Decision
36 days
Submission Type
Summary