Duo™ Lumbar Interbody Fusion Device

Duo™ Lumbar Interbody Fusion Device is an FDA 510(k)-cleared medical device (K181792) manufactured by Spineology, 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 August 13, 2018. Regulation: 8.