Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)

Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe) is an FDA 510(k)-cleared medical device (K180369) 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 September 13, 2018. Regulation: 8.