Vertera Spine Cohere Cervical Interbody Fusion Device

Vertera Spine Cohere Cervical Interbody Fusion Device is an FDA 510(k)-cleared medical device (K173030) manufactured by Nu Vasive, Incorporated. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 2017. Regulation: 8.