Intracept Intraosseous Nerve Ablation System

Intracept Intraosseous Nerve Ablation System is an FDA 510(k)-cleared medical device (K213836) manufactured by Relievant Medsystems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 10, 2022. Regulation: 8.