Vertera Spine™ Coalesce™ Thoracolumbar Interbody Fusion System

Vertera Spine™ Coalesce™ Thoracolumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K173153) 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 December 5, 2017. Regulation: 8.