TrellOss™-L MPF

TrellOss™-L MPF is an FDA 510(k)-cleared medical device (K192687) manufactured by Nexxt 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 January 8, 2020. Regulation: 8.