OIC Intramedullary Nail System

OIC Intramedullary Nail System is an FDA 510(k)-cleared medical device (K181184) manufactured by The Orthopaedic Implant Company. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 2018. Regulation: 8.