Relievant Medsystems is one of 25944 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Relievant Medsystems - FDA 510(k) Cleared Devices
Recent clearances: Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator, Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe), Relievant Medsystems RF Generator
6
Total
6
Cleared
0
Denied
Relievant Medsystems has 6 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 6 cleared submissions from 2010 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Relievant Medsystems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Boston Scientific Neuromodulation as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Relievant Medsystems
6 devices
Cleared
May 03, 2019
Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept...
Neurology
63d
Cleared
Sep 14, 2018
Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)
Neurology
214d
Cleared
Aug 18, 2017
Relievant Medsystems RF Generator
Neurology
122d
Cleared
Aug 09, 2017
INTRACEPT Intraosseous Nerve Ablation System
Neurology
142d
Cleared
CT
Jul 09, 2016
INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set
Neurology
240d
Cleared
Mar 30, 2010
INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND EASY ACCESS INSTRUMENT SET, MODEL...
General & Plastic Surgery
25d