Nalu Neurostimulation System for Peripheral Nerve Stimulation

FDA 510(k) K232415 · Boston Scientific Neuromodulation

Substantially Equivalent

510(k) numberK232415

Submission

Device name
Nalu Neurostimulation System for Peripheral Nerve Stimulation
Applicant
Boston Scientific Neuromodulation
Valencia, CA, US
Received
August 11, 2023
Decision date
August 21, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GZF – Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5870
Specialty
Neurology
Implant
Yes

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K243678TalisMann Neuromodulation SystemGZF · Traditional Bioventus, LLC07/03/2025SE
K233162Freedom Peripheral Nerve Stimulator (PNS) SystemGZF · Traditional Curonix06/20/2024SE
K221303Neuspera Nuity SystemGZF · Traditional Neuspera Medical, Inc.04/11/2023SE
K211965StimRouter Neuromodulation SystemGZF · Traditional Bioness, Inc.02/23/2022SE
K202781Neuspera Neurostimulation System (NNS)GZF · Traditional Neuspera Medical, Inc.08/27/2021SE
K200848Stimulator, Stimulator Kit, External Transmitter, External Transmitter KitGZF · Traditional Micron Medical Corporation08/14/2020SE
K200482StimRouter Neuromodulation SystemGZF · Special Bioness, Inc.03/27/2020SE
K190047StimRouter Neuromodulation SystemGZF · Traditional Bioness, Inc.10/31/2019SE

More from Bioness, Inc.

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K251247GX1 Radiofrequency Generator Kit (RFG-X1-120V); GX1 Radiofrequency Generator Kit…GXD · Traditional 08/07/2025SE
K233801Nalu Neurostimulation System for Spinal Cord Stimulation; Nalu Neurostimulation System…GZB · Traditional 08/23/2024SE
K221376Nalu Neurostimulation SystemGZB · Special 06/10/2022SE
K203547Nalu Neurostimulation SystemGZB · Traditional 03/25/2021SE
K202274Nalu Neurostimulation Kit (lnte:gmted 40 em: Single 8/Dual 8), Nalu Neurostimulation Kit…GZB · Traditional 11/09/2020SE
K201618Nalu Neurostimulation SCS systemGZB · Special 07/15/2020SE
K190960Nalu Lead Blank (50cm)GZB · Traditional 07/11/2019SE
K183579Nalu Neurostimulation Kit (Integrated, 40 cm: Single 8/Dual 8), Nalu Neurostimulation…GZF · Traditional 03/29/2019SE
K183047Nalu Neurostimulation SystemGZB · Traditional 03/22/2019SE

Questions and answers

When was Nalu Neurostimulation System for Peripheral Nerve Stimulation cleared by the FDA?

Nalu Neurostimulation System for Peripheral Nerve Stimulation (K232415) received a 510(k) decision of Substantially Equivalent on August 21, 2024, 376 days after the submission was received.

What is the product code of K232415?

The FDA product code is GZF – Stimulator, Peripheral Nerve, Implanted (Pain Relief), a Class II (moderate risk) device regulated under 21 CFR 882.5870.