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Arthrex TensionLoc System

Page Type
Cleared 510(K)
510(k) Number
K183628
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2019
Days to Decision
90 days
Submission Type
Summary

Arthrex TensionLoc System

Page Type
Cleared 510(K)
510(k) Number
K183628
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2019
Days to Decision
90 days
Submission Type
Summary