IVA & AEON Cervical and Lumbar Cage System

IVA & AEON Cervical and Lumbar Cage System is an FDA 510(k)-cleared medical device (K250335) manufactured by K&J Consulting. 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 28, 2025. Regulation: 8.