Mg OSTEOREVIVE™, Mg OSTEOCRETE™

Mg OSTEOREVIVE™, Mg OSTEOCRETE™ is an FDA 510(k)-cleared medical device (K242372) manufactured by Bone Solutions, 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 October 17, 2024. Regulation: 8.