FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implanted Brain Stimulator For Epilepsy

PMA: P100026 · Supplement: S088 · Decision Jan 18, 2022
Classifications
1
FEI Numbers
3
Registration Numbers
3

Basic Information

Device Name
Implanted Brain Stimulator For Epilepsy
Trade Name
NeuroPace® RNS® System
PMA Number
P100026
Supplement Number
S088
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
January 18, 2022
Date Received
October 28, 2021
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval to modify the labeling for the NeuroPace® RNS® Neurostimulator model RNS-320 to provide updated estimates for battery longevity.

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