FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implanted Brain Stimulator For Epilepsy

PMA: P100026 · Supplement: S075 · Decision Dec 17, 2019
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
S075
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
December 17, 2019
Date Received
September 30, 2019
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for 1) a firmware update (RAM 7.101) to the RNS Neurostimulator (model RNS-320) to disable Long Episode counting during telemetry; and 2) an adjustment to the crystal oscillator trim value (from 00h to 64h) on the neurostimulator to mitigate the possibility of the device unnecessarily transitioning into passive mode.

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