Last synced on 14 November 2025 at 11:06 pm

Arthrex Intramedullary Nails

Page Type
Cleared 510(K)
510(k) Number
K243890
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2025
Days to Decision
26 days
Submission Type
Summary

Arthrex Intramedullary Nails

Page Type
Cleared 510(K)
510(k) Number
K243890
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2025
Days to Decision
26 days
Submission Type
Summary