FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Permanent Defibrillator Electrodes
PMA: P920015
·
Supplement: S208
·
Decision Mar 20, 2018
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Permanent Defibrillator Electrodes
- Trade Name
- 6996T Tunneling Tool Sterile Barrier System
- PMA Number
- P920015
- Supplement Number
- S208
- Device Class
- FDA Class 3
- Product Code
- NVY
- Generic Name
- Permanent defibrillator electrodes
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- March 20, 2018
- Date Received
- February 22, 2018
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Addition of packaging and sterilization processes at the Rice Creek facility as well as minor process and sterilization changes for the Model 6996T tunneling tool.
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 |
|---|---|---|---|
| NVY | Permanent Defibrillator Electrodes | FDA class 3 | Unknown |