FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Permanent Defibrillator Electrodes
PMA: P920015
·
Supplement: S225
·
Decision Mar 5, 2019
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Permanent Defibrillator Electrodes
- Trade Name
- Sprint Quattro Secure and Sprint Quattro Secure S
- PMA Number
- P920015
- Supplement Number
- S225
- Device Class
- FDA Class 3
- Product Code
- NVY
- Generic Name
- Permanent defibrillator electrodes
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 5, 2019
- Date Received
- January 30, 2019
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Labeling Change - PAS
- Expedited Review
- N
Advisory Committee Statement
Approval for labeling updates to the clinical study summary for the post approval study.
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 |