Atlas Spine Rebar (Ti) Spacer System

Atlas Spine Rebar (Ti) Spacer System is an FDA 510(k)-cleared medical device (K202302) manufactured by Atlas Spine, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 29, 2020. Regulation: 8.