Atlas FDA

VNS THERAPY SYSTEM

FDA premarket approval P970003/S104 · decided 2009-07-23

Approval details

PMA number
P970003
Supplement
S104
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
VNS THERAPY SYSTEM
Generic name
Stimulator, autonomic nerve, implanted for epilepsy
Applicant
LivaNova USA, Inc.
Date received
2008-11-26
Decision date
2009-07-23
Days to decision
239 days
Decision code
APPR
Product code
LYJ
Advisory committee
Neurology
Expedited review
No
Location
Houston, TX
Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

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510(k) clearances by this applicant

RecordFirmDate
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