FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Autonomic Nerve, Implanted (Depression)

PMA: P970003 · Supplement: S190 · Decision Apr 29, 2016
Classifications
1
FEI Numbers
1
Registration Numbers
1

Basic Information

Device Name
Stimulator, Autonomic Nerve, Implanted (Depression)
Trade Name
VNS THERAPY SYSTEM
PMA Number
P970003
Supplement Number
S190
Device Class
FDA Class 3
Product Code
MUZ
Generic Name
Stimulator, autonomic nerve, implanted (depression)
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
Approved
Decision Code
APPR
Decision Date
April 29, 2016
Date Received
February 4, 2016
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for a new serial adapter cable to connect the programming computer to the programming wand.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUZ Stimulator, Autonomic Nerve, Implanted (Depression)