Avanti Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm Cannulated Screws, Avanti Orthopaedics Ulnar Shortening System, Avanti Distal Radius and Forearm System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Avanti Orthopaedics, Inc. Orthopedic ✕
3 devices