Expandable Titanium PLIF/TLIF System

Expandable Titanium PLIF/TLIF System is an FDA 510(k)-cleared medical device (K201024) manufactured by Spectrum Spine, 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 28, 2021. Regulation: 8.