FDA Review Panel · NE

FDA 510(k) Neurology Devices

About Neurology Devices

FDA 510(k) neurology devices cover diagnostic and therapeutic equipment for the nervous system. The FDA review panel code is NE.

Common categories include:

  • EEG and neurophysiology systems - electroencephalographs, EMG, nerve conduction
  • Neurostimulators - transcranial magnetic stimulation (TMS), vagus nerve stimulation
  • Surgical navigation systems - image-guided neurosurgery platforms
  • Intracranial pressure monitors - ICP sensors and drainage systems
  • Neuroendoscopes - rigid and flexible scopes for minimally invasive neurosurgery

133
Total
133
Cleared
165d
Avg days
2021
Since

FDA 510(k) Cleared Neurology Devices

This page lists all 133 medical devices in the Neurology specialty that have been submitted to the FDA through the 510(k) premarket notification process. EEG systems, neurostimulators, robotic surgical navigation and neuromonitoring.

  • 133 devices cleared as substantially equivalent to a predicate device.
  • Average time to FDA decision: 165 days.
  • Records available from 2021 to the present.
  • Filter by product code using the sidebar to narrow results by device type.
133 Neurology devices
1–12 of 133
Cleared Mar 16, 2026
Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)
K253447 · Orthocon, Inc.
GXR · Cover, Burr Hole · 165d
Cleared Mar 13, 2026
Permatage Flowable, Settable Bone Paste
K253732 · Orthocon, Inc.
GXP · Methyl Methacrylate For Cranioplasty · 109d
Cleared Mar 13, 2026
Visualase Cooled Laser Applicator System (9735559)
K253391 · Medtronic Navigation, Inc.
ONO · Neurosurgical Laser With Mr Thermography · 164d
Cleared Feb 13, 2026
STAR RF Ablation System
K251802 · Merit Medical Systems, Inc.
GXI · Probe, Radiofrequency Lesion · 246d
Cleared Feb 11, 2026
AXS Lift Intracranial Base Catheter
K253032 · Stryker Neurovascular
QJP · Catheter, Percutaneous, Neurovasculature · 142d
Cleared Feb 02, 2026
CHIKAI Nexus petit
K252011 · Asahi Intecc Co., Ltd.
MOF · Guide, Wire, Catheter, Neurovasculature · 220d
Cleared Jan 11, 2026
SafeOp 3: Neural Informatix System
K252842 · Alphatec Spine, Inc.
GWF · Stimulator, Electrical, Evoked Response · 125d
Cleared Jan 07, 2026
Materialise Personalized Guides and Models for Craniomaxillofacial Surgery CMF Titanium Guides
K253308 · Materialise NV
PPT · Cranial Surgical Planning And Instrument Guides · 100d
Cleared Jan 02, 2026
MONTAGE XT Cranial Cement
K253854 · Orthocon, Inc.
GXP · Methyl Methacrylate For Cranioplasty · 30d
Cleared Dec 11, 2025
Target Detachable Coil
K252694 · Stryker Neurovascular
HCG · Device, Neurovascular Embolization · 107d
Cleared Nov 21, 2025
Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4
K251856 · Everyway Medical Instruments Co.,Ltd
NUH · Stimulator, Nerve, Transcutaneous, Over-the-counter · 157d
Cleared Nov 18, 2025
Collagen Dura Regeneration Membrane - Repair
K251191 · Collagen Matrix, Inc.
GXQ · Dura Substitute · 215d

How to use this database

This page lists 133 medical devices in the Neurology specialty submitted to the FDA through the 510(k) premarket notification process. Of these, 133 were cleared as substantially equivalent to a predicate device. Average FDA review time: 165 days. Records from 2021 to the present.

You can use this list to:

  • Find predicate devices for a new 510(k) submission
  • Verify the clearance status of a specific device
  • Identify FDA product codes related to neurology
  • Compare similar cleared devices within this category
  • Research manufacturers active in this specialty

Each entry includes: device name, 510(k) number, product code, manufacturer and FDA decision date. Click any device to view the full submission details.

This information is based on publicly available FDA data and is intended for informational purposes only. It may not reflect current market or regulatory status. Always verify critical information at accessdata.fda.gov.

Looking for a specific neurology device? Search by device name, K-number or manufacturer.

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