FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Implanted Brain Stimulator For Epilepsy

PMA: P100026 · Supplement: S030 · Decision Mar 6, 2015
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
S030
Device Class
FDA Class 3
Product Code
PFN
Generic Name
Implanted brain stimulator for epilepsy
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
March 6, 2015
Date Received
February 6, 2015
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

MODIFY THE MANUFACTURING AND INSPECTION PROCESS FOR THE WAND (W-2).

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