Osteo-P Bone Graft Substitute

Osteo-P Bone Graft Substitute is an FDA 510(k)-cleared medical device (K170165) manufactured by Molecular Matrix, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 28, 2017. Regulation: 8.