Advantage-C? Ti3D Cervical Interbody Fusion Device
Jan 2026
134d
Intelivation Technologies
1
Total
1
Cleared
0
Denied
Intelivation Technologies — FDA 510(k) Submissions
Intelivation Technologies has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Cervical . Use the specialty filter in the sidebar to narrow results.
1 devices