VNS Therapy System
FDA premarket approval P970003/S229 · decided 2020-01-13
Approval details
- PMA number
- P970003
- Supplement
- S229
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- VNS Therapy System
- Generic name
- Stimulator, autonomic nerve, implanted for epilepsy
- Applicant
- LivaNova USA, Inc.
- Date received
- 2019-10-15
- Decision date
- 2020-01-13
- Days to decision
- 90 days
- Decision code
- APPR
- Product code
- LYJ
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Houston, TX
- Statement
- Approval for the changes that are being made to the firmware of the Model 1000 Generator (SN >= 100,000) to prevent resetting the microcontroller unit when an uncorrectable FRAM bit error is detected.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| Venous Return Cannulae (K250937) | LivaNova USA, Inc. | 2026-03-11 |
| RAP Femoral Venous Cannulae (K250283) | LivaNova USA, Inc. | 2025-07-10 |
| SMARxT Tubing and Connectors (K233702) | LivaNova USA, Inc. | 2024-08-08 |