Last synced on 25 January 2026 at 3:41 am

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203268
510(k) Type
Special
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2020
Days to Decision
22 days
Submission Type
Summary

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203268
510(k) Type
Special
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2020
Days to Decision
22 days
Submission Type
Summary