PMA
P090013: REVO MRI SURESCAN IPG AND PACING SYSTEM
FDA PMA · Implantable pulse generator, pacemaker (non-CRT) · Medtronic, Inc.
Key facts
| PMA number | P090013 |
|---|---|
| Trade name | REVO MRI SURESCAN IPG AND PACING SYSTEM |
| Generic name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | Medtronic, Inc. |
| Owner/operator | Medtronic, Inc. |
| Product code | LWP |
| Approval date | Feb 8, 2011 |
| Docket number | 11M-0105 |
| Notice date | Feb 24, 2011 |
| Establishment registration | 2182208 |
| FEI number | 2182208 |
At a glance
- 100–999 Supplements
- Jun 5, 2025 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: