FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Cochlear
PMA: P960058
·
Supplement: S022
·
Decision Jun 6, 2002
Classifications
1
FEI Numbers
22
Registration Numbers
22
Basic Information
- Device Name
- Implant, Cochlear
- Trade Name
- BTE(BEHIND-THE-EAR)SYSTEM SENSOR (PEDIATRIC)
- PMA Number
- P960058
- Supplement Number
- S022
- Device Class
- FDA Class 3
- Product Code
- MCM
- Generic Name
- Implant, cochlear
- Medical Specialty
- Unknown
- Advisory Committee
- Ear, Nose, Throat
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 6, 2002
- Date Received
- May 28, 2002
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE BTE SYSTEM SENSOR, AN ACCESSORY ITEM TO BE OFFERED FOR USE WITH THE BTE SOUND PROCESSOR FOR LIMITED VERIFICATION OF SYSTEM FUNCTIONALITY.
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 |
|---|---|---|---|
| MCM | Implant, Cochlear | FDA class 3 | Unknown |