PMA supplement
P100040 S036: Valiant Navion Thoracic Stent Graft System
FDA PMA supplement · Panel Track · Medtronic Vascular
Key facts
| Original PMA | P100040 |
|---|---|
| Supplement number | S036 |
| Supplement type | Panel Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | Valiant Navion Thoracic Stent Graft System |
| Generic name | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT |
| Applicant | Medtronic Vascular |
| Product code | MIH |
| Received date | Apr 23, 2018 |
| Decision date | Oct 19, 2018 |
| Docket number | 18M-4033 |
| Notice date | Oct 25, 2018 |
At a glance
- No Expedited review granted
- Yes Approval order on file
- Yes 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: