Last synced on 14 November 2025 at 11:06 pm

KNOTLESS FIBERTAK SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K130458
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2013
Days to Decision
70 days
Submission Type
Summary

KNOTLESS FIBERTAK SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K130458
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2013
Days to Decision
70 days
Submission Type
Summary