Invictus™ OsseoScrew® System

Invictus™ OsseoScrew® System is an FDA 510(k)-cleared medical device (K202327) manufactured by Alphatec Spine, 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 14, 2020. Regulation: 8.