FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

PMA: P840001 · Supplement: S022 · Decision Jan 17, 1992
Classifications
1
FEI Numbers
55
Registration Numbers
55

Basic Information

Device Name
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Trade Name
MEDTRONIC ITREL SPINAL CORD STIMULATION SYSTEM
PMA Number
P840001
Supplement Number
S022
Device Class
FDA Class 3
Product Code
LGW
Generic Name
Stimulator, spinal-cord, totally implanted for pain relief
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
Approved
Decision Code
APPR
Decision Date
January 17, 1992
Date Received
September 4, 1990
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Classifications

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

Product Code Device Name
LGW Stimulator, Spinal-Cord, Totally Implanted For Pain Relief