CancelleX Porous Titanium Lumbar Interbody Device

CancelleX Porous Titanium Lumbar Interbody Device is an FDA 510(k)-cleared medical device (K190364) manufactured by Xenco Medical, 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 17, 2019. Regulation: 8.