Last synced on 12 October 2025 at 8:21 pm

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251809
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2025
Days to Decision
36 days
Submission Type
Summary

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251809
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2025
Days to Decision
36 days
Submission Type
Summary