Spinal Elements, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ventana® P/T Lumbar Interbody System, Ventana™ A Anterior Lumbar Interbody System, Luna® Ti Interbody Fusion System
49
Total
49
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spinal Elements, Inc. General & Plastic Surgery ✕
1 devices