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 | Device Class | Medical Specialty |
|---|---|---|---|
| PFN | Implanted Brain Stimulator For Epilepsy | FDA class 3 | Unknown |