MONTAGE Settable, Resorbable Bone Putty

MONTAGE Settable, Resorbable Bone Putty is an FDA 510(k)-cleared medical device (K221933) manufactured by Orthocon, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 12, 2023. Regulation: 8.