FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
PMA: P830061
·
Supplement: S168
·
Decision May 30, 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 Sense MRI SureScan Lead
- PMA Number
- P830061
- Supplement Number
- S168
- 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
- Approved
- Decision Code
- APPR
- Decision Date
- May 30, 2019
- Date Received
- May 2, 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 |
|---|---|---|---|
| NVN | Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes | FDA class 3 | Unknown |