FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Permanent Defibrillator Electrodes
PMA: P920015
·
Supplement: S259
·
Decision Aug 17, 2021
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Permanent Defibrillator Electrodes
- Trade Name
- Y Adaptor/Extender Kit, DF-1 Connector Port Pin Plug, HV Splitter/Adaptor Kit, IS-1 Connector Port Pin Plug Kit, Lead Ad
- PMA Number
- P920015
- Supplement Number
- S259
- 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
- August 17, 2021
- Date Received
- August 9, 2021
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Minor modifications, including new ovens and a new toolmaker's scope at Medtronic Rice Creek.
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 |