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