Montage Flowable Settable, Resorbable Bone Paste

Montage Flowable Settable, Resorbable Bone Paste is an FDA 510(k)-cleared medical device (K232771) 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 February 15, 2024. Regulation: 8.