Caliber Intramedullary Fixation System

Caliber Intramedullary Fixation System is an FDA 510(k)-cleared medical device (K242896) manufactured by Nvision Biomedical Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 2025. Regulation: 8.