Spinal Jaxx Interbody Fusion Device

Spinal Jaxx Interbody Fusion Device is an FDA 510(k)-cleared medical device (K152501) manufactured by Neuropro Spinaljaxx, 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 June 28, 2016. Regulation: 8.