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Knotless SutureTak Anchors

Page Type
Cleared 510(K)
510(k) Number
K180594
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2018
Days to Decision
108 days
Submission Type
Summary

Knotless SutureTak Anchors

Page Type
Cleared 510(K)
510(k) Number
K180594
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2018
Days to Decision
108 days
Submission Type
Summary