Orthosoft D/B/A Zimmer Cas - FDA 510(k) Cleared Devices
Recent clearances: ROSA Partial Knee System, ROSA® Knee System, ROSA® Knee System
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Orthosoft D/B/A Zimmer Cas Radiology ✕
2 devices