K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage

K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage is an FDA 510(k)-cleared medical device (K212038) manufactured by K&J Consulting Corporation. 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 26, 2021. Regulation: 8.