EL CAPITAN Anterior Lumbar Interbody Fusion

EL CAPITAN Anterior Lumbar Interbody Fusion is an FDA 510(k)-cleared medical device (K222554) manufactured by Astura Medical. 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 18, 2023. Regulation: 8.