Last synced on 14 November 2025 at 11:06 pm

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K200341
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2020
Days to Decision
30 days
Submission Type
Summary

Arthrex FiberTak Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K200341
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2020
Days to Decision
30 days
Submission Type
Summary