Calix Lumbar Spinal Implant System

Calix Lumbar Spinal Implant System is an FDA 510(k)-cleared medical device (K170119) manufactured by X-Spine Systems, 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 September 28, 2017. Regulation: 8.