FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

PMA: P840001 · Supplement: S346 · Decision Dec 13, 2016
Classifications
1
FEI Numbers
55
Registration Numbers
55

Basic Information

Device Name
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Trade Name
SCS ACCESSORIES, SCS EXTENSIONS, SCS LEADS, SCS LEADS 1x8 FAMILY, SCS LEADS PISCES FAMILY, SCS LEADS RESUME FAMILY, SCS
PMA Number
P840001
Supplement Number
S346
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
30-Day Notice Accepted
Decision Code
OK30
Decision Date
December 13, 2016
Date Received
November 14, 2016
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Update of the manufacturing execution system (MES) to FACTORYworks (FW) Release 9.3.

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