Last synced on 14 November 2025 at 11:06 pm

Cannulated Screw and Kirschner (K wire) System

Page Type
Cleared 510(K)
510(k) Number
K252758
510(k) Type
Special
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2025
Days to Decision
34 days
Submission Type
Summary

Cannulated Screw and Kirschner (K wire) System

Page Type
Cleared 510(K)
510(k) Number
K252758
510(k) Type
Special
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2025
Days to Decision
34 days
Submission Type
Summary