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 | Device Class | Medical Specialty |
|---|---|---|---|
| GZC | Stimulator, Neuromuscular, Implanted | FDA class 3 | Neurology |