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Arthrex Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K240815
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2024
Days to Decision
80 days
Submission Type
Summary

Arthrex Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K240815
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2024
Days to Decision
80 days
Submission Type
Summary