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FiberTak® Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K231330
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2023
Days to Decision
24 days
Submission Type
Summary

FiberTak® Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K231330
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2023
Days to Decision
24 days
Submission Type
Summary