FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Stimulator, Autonomic Nerve, Implanted For Epilepsy
PMA: P970003
·
Supplement: S252
·
Decision Dec 17, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Stimulator, Autonomic Nerve, Implanted For Epilepsy
- Trade Name
- VNS THERAPY SYSTEM
- PMA Number
- P970003
- Supplement Number
- S252
- Device Class
- FDA Class 3
- Product Code
- LYJ
- Generic Name
- Stimulator, autonomic nerve, implanted for epilepsy
- Medical Specialty
- Unknown
- Advisory Committee
- Neurology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- December 17, 2025
- Date Received
- November 17, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
to implement a new burn-in process for the MSP430 Microcontrollers at a supplier for the Models 100 and 1000-D, SenTiva Implantable Pulse Generators
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 |
|---|---|---|---|
| LYJ | Stimulator, Autonomic Nerve, Implanted For Epilepsy | FDA class 3 | Unknown |