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Univers Revers Modular Glenoid System, Half Augment Baseplate

Page Type
Cleared 510(K)
510(k) Number
K200895
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2020
Days to Decision
132 days
Submission Type
Summary

Univers Revers Modular Glenoid System, Half Augment Baseplate

Page Type
Cleared 510(K)
510(k) Number
K200895
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2020
Days to Decision
132 days
Submission Type
Summary