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Arthrex Knee FiberTak® Button Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K232973
510(k) Type
Traditional
Applicant
Arthrex Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2023
Days to Decision
55 days
Submission Type
Summary

Arthrex Knee FiberTak® Button Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K232973
510(k) Type
Traditional
Applicant
Arthrex Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2023
Days to Decision
55 days
Submission Type
Summary