Atlas FDA

VNS THERAPY SYSTEM

FDA premarket approval P970003/S150 · decided 2012-07-26

Approval details

PMA number
P970003
Supplement
S150
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VNS THERAPY SYSTEM
Generic name
Stimulator, autonomic nerve, implanted (depression)
Applicant
LivaNova USA, Inc.
Date received
2012-07-02
Decision date
2012-07-26
Days to decision
24 days
Decision code
OK30
Product code
MUZ
Advisory committee
Neurology
Expedited review
No
Location
Houston, TX
Statement
UPDATES TO THE ELECTRICAL TEST SYSTEM SOFTWARE FOR VARIOUS MODELS OF THE VNS THERAPY SYSTEM PULSE GENERATORS.

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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