NeoSpan® Compression Implant System

NeoSpan® Compression Implant System is an FDA 510(k)-cleared medical device (K233089) manufactured by In2bones USA, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 23, 2024. Regulation: 8.