Relievant Medsystems

FDA Filings

This page includes the latest FDA filings for Relievant Medsystems. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3006789852
FEI Number3006789852
NameRelievant MedSystems
Owner & OperatorRelievant Medsystems
Contact Address1230 Midas Way, Suite 200
Sunnyvale CA 94085 US
Official Correspondent
  • Mark Smutka
  • x-650-3681000-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1230 Midas Way, Suite 200
Sunnyvale, CA 94085 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
Relievant Medsystems
Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator2019-05-03
Relievant Medsystems
Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)2018-09-14
Relievant MedSystems
RF Generator2017-09-21
Relievant Medsystems
Relievant Medsystems RF Generator2017-08-18
Relievant Medsystems
INTRACEPT Intraosseous Nerve Ablation System2017-08-09
RELIEVANT MEDSYSTEMS
INTRACEPT Flexible Bi-Polar RF Probe And Easy Access Instrument Set2016-07-09
Relievant MedSystems
INTRACEPT Flexible Bi-Polar RF Probe & Easy Access Instrumen2010-12-22
Relievant MedSystems
INTRACEPT Flexible Bi-Polar RF Probe & Curved Instrument Set2010-12-22
RELIEVANT MEDSYSTEMS
INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND EASY ACCESS INSTRUMENT SET, MODEL FG0018 (PROBE), FG0036 (INSTRUMENT SET)2010-03-30
Relievant MedSystems
INTRACEPT Bi-Polar RF Probe2007-10-29

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Related Finance Registrations
NCAGE Code5EPY4RELIEVANT MEDSYSTEMS
CAGE Code5EPY4RELIEVANT MEDSYSTEMS
DUNS006233149RELIEVANT MEDSYSTEMS
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