VNS THERAPY DEMIPULSE/DEMIPULSE DUO GENERATORS
FDA premarket approval P970003/S125 · decided 2011-04-29
Approval details
- PMA number
- P970003
- Supplement
- S125
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VNS THERAPY DEMIPULSE/DEMIPULSE DUO GENERATORS
- Generic name
- Stimulator, autonomic nerve, implanted for epilepsy
- Applicant
- LivaNova USA, Inc.
- Date received
- 2011-03-31
- Decision date
- 2011-04-29
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LYJ
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Houston, TX
- Statement
- MODIFICATION OF VISUAL INSPECTION ACCEPTANCE CRITERIA FOR THREE CAPACITORS
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510(k) clearances by this applicant
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|---|---|---|
| Venous Return Cannulae (K250937) | LivaNova USA, Inc. | 2026-03-11 |
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