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Arthrex Univers Revers Shoulder Prosthesis System

Page Type
Cleared 510(K)
510(k) Number
K161782
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2016
Days to Decision
145 days
Submission Type
Summary

Arthrex Univers Revers Shoulder Prosthesis System

Page Type
Cleared 510(K)
510(k) Number
K161782
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2016
Days to Decision
145 days
Submission Type
Summary