FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Implanted Brain Stimulator For Epilepsy
PMA: P100026
·
Supplement: S060
·
Decision Oct 5, 2018
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
- S060
- 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
- October 5, 2018
- Date Received
- October 3, 2018
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
NeuroPace's battery supplier, Integer, to use an alternate supplier (second tier) to procure electrolyte used in batteries for RNS Neurostimulator model RNS-300M and model RNS-320.
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 |