Relievant Medsystems, Inc. is one of 16343 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Relievant Medsystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Intracept Intraosseous Nerve Ablation System, Intracept Intraosseous Nerve Ablation System, INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
4
Total
4
Cleared
0
Denied
Relievant Medsystems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Hayward, US.
Last cleared in 2022. Active since 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Relievant Medsystems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Boston Scientific Neuromodulation as regulatory consultant.
FDA 510(k) Regulatory Record - Relievant Medsystems, Inc.
4 devices
Cleared
Oct 26, 2022
Intracept Intraosseous Nerve Ablation System
Neurology
89d
Cleared
Mar 11, 2022
Intracept Intraosseous Nerve Ablation System
Neurology
92d
Cleared
Jan 22, 2009
INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS:...
General & Plastic Surgery
29d
Cleared
Oct 05, 2007
INTRACEPT BI-POLAR RF PROBE, MODEL 04814
General & Plastic Surgery
232d