# Medtronic, Inc.: PMA supplement approved for Aurora EV ICD DVEA3E4

**Score:** 30/100

| Field | Value |
|---|---|
| Sponsor | Medtronic, Inc. |
| Product | Aurora EV ICD DVEA3E4 |
| Generic / ingredient | Implantable cardioverter defibrillator (non-CRT) |
| Approval | PMA supplement (device change) |
| Application | P220012 S069 |
| Decided | 2026-06-25 |
| Panel / class | Cardiovascular |
| Sponsor location | Mounds View, MN |

## Why this score


Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P220012S069). Last refreshed: 2026-11-05T08:47:15.055Z.
From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.