uCerv Flux-C 3D Porous Titanium Cervical Interbody

uCerv Flux-C 3D Porous Titanium Cervical Interbody is an FDA 510(k)-cleared medical device (K220696) manufactured by Ulrich Medical USA. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 2022. Regulation: 8.