FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implanted Brain Stimulator For Epilepsy

PMA: P100026 · Supplement: S063 · Decision Sep 19, 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
S063
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
September 19, 2019
Date Received
February 6, 2019
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for the current NeuroPace supplier of the Tunneling Tool Straw (Straw), Teleflex Medical OEM (located at 50 Plantation Drive, Jaffrey NH 03452), to source raw polytetrafluoroethylene (PTFE) resin used in the Straw manufacture from an alternate supplier.

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