FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Permanent Defibrillator Electrodes
PMA: P980023
·
Supplement: S113
·
Decision Jan 20, 2023
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Permanent Defibrillator Electrodes
- Trade Name
- Pamira ICD Leads
- PMA Number
- P980023
- Supplement Number
- S113
- 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
- January 20, 2023
- Date Received
- May 19, 2022
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for design changes to the Plexa lead family, resulting in the Pamira lead family.
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 |