PEEK CAGE FOR THE VERTEBRAL SPINE

PEEK CAGE FOR THE VERTEBRAL SPINE is an FDA 510(k)-cleared medical device (K132852) manufactured by Neoortho Produtos Ortopedicos S/A. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 2014. Regulation: 8.