PULSE GENERATOR-MODEL102, PULSE DUO GENERATOR-MODEL 102R
FDA premarket approval P970003/S179 · decided 2015-08-21
Approval details
- PMA number
- P970003
- Supplement
- S179
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- PULSE GENERATOR-MODEL102, PULSE DUO GENERATOR-MODEL 102R
- Generic name
- Stimulator, autonomic nerve, implanted for epilepsy
- Applicant
- LivaNova USA, Inc.
- Date received
- 2015-05-26
- Decision date
- 2015-08-21
- Days to decision
- 87 days
- Decision code
- APPR
- Product code
- LYJ
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Houston, TX
- Statement
- APPROVAL FOR THE INTRODUCTION OF AN ALTERNATE MICROPROCESSOR, MANUFACTURED BY A DIFFERENT VENDOR, FOR THE MODEL 102/102R PULSE GENERATORS USED IN THE VNS THERAPY SYSTEM.
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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 |