FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Neuromuscular, Implanted

PMA: P950035 · Supplement: S010 · Decision Sep 13, 2001
Classifications
1
FEI Numbers
0
Registration Numbers
0

Basic Information

Device Name
Stimulator, Neuromuscular, Implanted
Trade Name
NEUROCONTROL FREEHAND SYSTEM
PMA Number
P950035
Supplement Number
S010
Device Class
FDA Class 3
Product Code
GZC
Generic Name
Stimulator, neuromuscular, implanted
Regulation Number
882.5860
Medical Specialty
Neurology
Advisory Committee
Ear, Nose, Throat
Decision
Approved
Decision Code
APPR
Decision Date
September 13, 2001
Date Received
August 14, 2001
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR REVISIONS TO THE LABELING THAT SPECIFY THE MAXIMUM DEPTH BELOW THE SURFACE OF THE SKIN AT WHICH THE IMPLANTABLE RECEIVER-STIMULATOR (IRS) SHOULD NOT EXCEED WHEN IMPLANTED AND CLARIFYING THE INSTRUCTIONS FOR CONNECTING THE EXTERNAL CONTROLLER TO THE CLINICAL PROGRAMMING STATION.

Classifications

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

Product Code Device Name
GZC Stimulator, Neuromuscular, Implanted