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Arthrex PushLock Tenodesis Anchor

Page Type
Cleared 510(K)
510(k) Number
K181513
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2018
Days to Decision
83 days
Submission Type
Summary

Arthrex PushLock Tenodesis Anchor

Page Type
Cleared 510(K)
510(k) Number
K181513
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2018
Days to Decision
83 days
Submission Type
Summary