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Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K231113
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2023
Days to Decision
29 days
Submission Type
Summary

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K231113
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2023
Days to Decision
29 days
Submission Type
Summary