Ceterix Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0), NovoStitch Pro Meniscal Repair System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ceterix Orthopaedics, Inc. General & Plastic Surgery ✕
3 devices