Stimpod NMS450 Nerve Stimulator

FDA 510(k) K102084 · Xavant Technology (Pty), Ltd.

Substantially Equivalent

510(k) numberK102084

Submission

Device name
Stimpod NMS450 Nerve Stimulator
Applicant
Xavant Technology (Pty), Ltd.
Pretoria, Gauteng, ZA
Received
July 26, 2010
Decision date
December 16, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
BXN – Stimulator, Nerve, Battery-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 868.2775
Specialty
Anesthesiology

Other 510(k)s with product code BXN

510(k)DeviceApplicantDecision
K213049STIMPOD NMS450 Nerve StimulatorBXN · Traditional Xavant Technology (Pty), Ltd.10/16/2022SE
K162086MultiStim ECOBXN · Traditional PAJUNK GmbH Medizintechnologie01/06/2017SE
K153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorBXN · Special Easy Med Instrument Co., Ltd.05/13/2016SE
K143095MiniStim MS-IVB Peripheral Nerve StimulatorBXN · Traditional Halyard Health, Inc.03/24/2015SE
K140853Stimpod ST2-3010 Nerve StimulatorBXN · Special Xavant Technology (Pty), Ltd.11/06/2014SE
K121743Easymed Peripheral Nerve Stimulator-SunstinBXN · Traditional Sunmed, LLC03/28/2013SE
K111985Myoguide System Model 8008BXN · Traditional Intronix Technologies Corp.12/30/2011SE
K110118Stimtrode Single Use Nerve StimulatorBXN · Special Xavant Technology (Pty), Ltd.02/17/2011SE
K093591Stimpod Model NMS-400 Nerve StimulatorBXN · Traditional Xavant Technology (Pty), Ltd.12/03/2009SE
K091155AscendBXN · Traditional Neurometrix, Inc.09/03/2009SE

More from Neurometrix, Inc.

510(k)DeviceDecision
K213049STIMPOD NMS450 Nerve StimulatorBXN · Traditional 10/16/2022SE
K161091STIMPOD NMS460 Nerve StimulatorGZJ · Traditional 01/18/2017SE
K140853Stimpod ST2-3010 Nerve StimulatorBXN · Special 11/06/2014SE
K110118Stimtrode Single Use Nerve StimulatorBXN · Special 02/17/2011SE
K093591Stimpod Model NMS-400 Nerve StimulatorBXN · Traditional 12/03/2009SE
K072092Xpod/Xmap Nerve StimulatorBXN · Traditional 11/15/2007SE

Questions and answers

When was Stimpod NMS450 Nerve Stimulator cleared by the FDA?

Stimpod NMS450 Nerve Stimulator (K102084) received a 510(k) decision of Substantially Equivalent on December 16, 2010, 143 days after the submission was received.

What is the product code of K102084?

The FDA product code is BXN – Stimulator, Nerve, Battery-Powered, a Class II (moderate risk) device regulated under 21 CFR 868.2775.