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Arthrex Univers Revers Modular Glenoid System

Page Type
Cleared 510(K)
510(k) Number
K191960
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
153 days
Submission Type
Summary

Arthrex Univers Revers Modular Glenoid System

Page Type
Cleared 510(K)
510(k) Number
K191960
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
153 days
Submission Type
Summary