Ventana™ A Anterior Lumbar Interbody System

Ventana™ A Anterior Lumbar Interbody System is an FDA 510(k)-cleared medical device (K253559) manufactured by Spinal Elements, 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 February 24, 2026. Regulation: 8.