Medical Device Manufacturer · US , Redwood City , CA

Relievant Medsystems - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2010

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)

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.

Relievant Medsystems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Relievant Medsystems

6 devices

1-6 of 6

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 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