VeriFixx™ Small Bone Implant

VeriFixx™ Small Bone Implant is an FDA 510(k)-cleared medical device (K202777) manufactured by Armis Biopharma, 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 November 16, 2020. Regulation: 8.