Stuckenbrock Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: IXOS Radius Plate System, HBS2 Headless Bone Screw
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stuckenbrock Medizintechnik GmbH Orthopedic ✕
3 devices