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Arthrex SwiveLock Anchors

Page Type
Cleared 510(K)
510(k) Number
K180768
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
266 days
Submission Type
Summary

Arthrex SwiveLock Anchors

Page Type
Cleared 510(K)
510(k) Number
K180768
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
266 days
Submission Type
Summary