
Trans1 Incorporated
Free shipping on orders over $99 · 30-day returns
TRANS1 INTERBODY FUSION SYSTEM is an FDA 510(k)-cleared medical device (K120991) manufactured by Trans1 Incorporated. 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 22, 2012. Regulation: 8.