INTRACEPT Intraosseous Nerve Ablation System

INTRACEPT Intraosseous Nerve Ablation System is an FDA 510(k)-cleared medical device (K170827) manufactured by Relievant Medsystems. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 8, 2017. Regulation: 8.