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Arthrex Knotless SutureTak Anchor

Page Type
Cleared 510(K)
510(k) Number
K171020
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2017
Days to Decision
41 days
Submission Type
Summary

Arthrex Knotless SutureTak Anchor

Page Type
Cleared 510(K)
510(k) Number
K171020
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2017
Days to Decision
41 days
Submission Type
Summary