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Arthrex Modular Glenoid System-Titanium Glenosphere

Page Type
Cleared 510(K)
510(k) Number
K212415
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2021
Days to Decision
106 days
Submission Type
Summary

Arthrex Modular Glenoid System-Titanium Glenosphere

Page Type
Cleared 510(K)
510(k) Number
K212415
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2021
Days to Decision
106 days
Submission Type
Summary