Last synced on 18 April 2025 at 11:05 pm

Arthrex Humeral Plating System and Cerclage Button

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243995
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2025
Days to Decision
90 days
Submission Type
Summary

Arthrex Humeral Plating System and Cerclage Button

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243995
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2025
Days to Decision
90 days
Submission Type
Summary