FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implanted Brain Stimulator For Epilepsy

PMA: P100026 · Supplement: S101 · Decision May 28, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0

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Basic Information

Device Name
Implanted Brain Stimulator For Epilepsy
Trade Name
NeuroPace® RNS® System
PMA Number
P100026
Supplement Number
S101
Device Class
FDA Class 3
Product Code
PFN
Generic Name
Implanted brain stimulator for epilepsy
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
Approved
Decision Code
APPR
Decision Date
May 28, 2026
Date Received
August 6, 2025
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

approval for an optional Electrocorticogram (ECoG) Assistant function, which is a clinician tool that highlights ECoG recordings of interest, for the Patient Data Management System.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PFN Implanted Brain Stimulator For Epilepsy