Kyocera Medical Technologies Inc. (KMTI) - FDA 510(k) Cleared Devices
Recent clearances: Varion Thoracolumbar Fixation System, Skyway Anterior Cervical Plate System, Skyway Anterior Cervical Plate System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kyocera Medical Technologies Inc. (KMTI) Orthopedic ✕
3 devices