Alcantara Thoracolumbar Plate System

Alcantara Thoracolumbar Plate System is an FDA 510(k)-cleared medical device (K232256) manufactured by Camber Spine Technologies, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 15, 2024. Regulation: 8.