FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

PMA: P010032 · Supplement: S087 · Decision Feb 12, 2015
Classifications
1
FEI Numbers
55
Registration Numbers
55

Basic Information

Device Name
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Trade Name
ST. JUDE MEDICAL ADAPTER
PMA Number
P010032
Supplement Number
S087
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
February 12, 2015
Date Received
November 18, 2014
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR MINOR LABELING CHANGES TO THE SJM 8-CHANNEL ADAPTOR (MODELS 2311 AND 2316); SPECIFICALLY, TO INCLUDE THE USE OF THE ADAPTOR WITH THE SJM TRIAL SYSTEM.

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