Spineex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices, SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices, SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spineex, Inc. Orthopedic ✕
3 devices