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Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay

Page Type
Cleared 510(K)
510(k) Number
K182039
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2018
Days to Decision
60 days
Submission Type
Summary

Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay

Page Type
Cleared 510(K)
510(k) Number
K182039
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2018
Days to Decision
60 days
Submission Type
Summary