FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
PMA: P950024
·
Supplement: S086
·
Decision Jul 2, 2019
Classifications
1
FEI Numbers
26
Registration Numbers
26
Basic Information
- Device Name
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
- Trade Name
- CapSure Epicardial Pacing Lead
- PMA Number
- P950024
- Supplement Number
- S086
- Device Class
- FDA Class 3
- Product Code
- NVN
- Generic Name
- Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 2, 2019
- Date Received
- June 21, 2019
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Transfer electrode assemblies from the Medtronic Energy and Component Center facility to the Medtronic Rice Creek and Medtronic Puerto Rico Operations Company facilities for completion and final inspection.
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 |
|---|---|---|---|
| NVN | Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes | FDA class 3 | Unknown |