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Arthrex Knotless AC Repair Devices

Page Type
Cleared 510(K)
510(k) Number
K220947
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2022
Days to Decision
66 days
Submission Type
Summary

Arthrex Knotless AC Repair Devices

Page Type
Cleared 510(K)
510(k) Number
K220947
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2022
Days to Decision
66 days
Submission Type
Summary