Spineology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OptiMesh Multiplanar Expandable Interbody Fusion System, Spineology Navigation Instruments, OptiMesh Multiplanar Expandable Interbody Fusion System
54
Total
51
Cleared
1
Denied
FDA 510(k) Regulatory Record - Spineology, Inc. General & Plastic Surgery ✕
1 devices