Atlas FDA

VNS THERAPY SYSTEM

FDA premarket approval P970003/S059 · decided 2005-11-08

Approval details

PMA number
P970003
Supplement
S059
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
VNS THERAPY SYSTEM
Generic name
Stimulator, autonomic nerve, implanted for epilepsy
Applicant
LivaNova USA, Inc.
Date received
2005-08-12
Decision date
2005-11-08
Days to decision
88 days
Decision code
APPR
Product code
LYJ
Advisory committee
Neurology
Expedited review
No
Location
Houston, TX
Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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