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Arthrex SwiveLock Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K191226
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2019
Days to Decision
35 days
Submission Type
Summary

Arthrex SwiveLock Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K191226
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2019
Days to Decision
35 days
Submission Type
Summary