Relievant Medsystems, Inc.

Relievant Medsystems, Inc. holds 4 FDA 510(k) medical device clearances, first cleared 2007, most recent 2022.

Top product codes for Relievant Medsystems, Inc.

GEI — General, Plastic Surgery2 devices
GXI — Neurology2 devices

Recent clearances by Relievant Medsystems, Inc.

K222281 — Intracept Intraosseous Nerve Ablation SystemCode GXI·2022-10-26
K213836 — Intracept Intraosseous Nerve Ablation SystemCode GXI·2022-03-11
K083856 — INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026Code GEI·2009-01-22
K070443 — INTRACEPT BI-POLAR RF PROBE, MODEL 04814Code GEI·2007-10-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.