PMA supplement
P980016 S722: Evera S DR/VR ICd, Evera XT DR/VR ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Mirro MRI DR/VR ICD, and Primo MRI DR/VR ICD
FDA PMA supplement · Real-Time Process · Medtronic Cardiac Rhythm Disease Management
Key facts
| Original PMA | P980016 |
|---|---|
| Supplement number | S722 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | Evera S DR/VR ICd, Evera XT DR/VR ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Mirro MRI DR/VR ICD, and Primo MRI DR/VR ICD |
| Generic name | Implantable cardioverter defibrillator (non-CRT) |
| Applicant | Medtronic Cardiac Rhythm Disease Management |
| Product code | LWS |
| Received date | Oct 15, 2019 |
| Decision date | Dec 16, 2019 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: