PMA supplement
P180029 S022: LOTUS Edge Valve System
FDA PMA supplement · Real-Time Process · Boston Scientific Corporation
Key facts
| Original PMA | P180029 |
|---|---|
| Supplement number | S022 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | LOTUS Edge Valve System |
| Generic name | Aortic valve, prosthesis, percutaneously delivered |
| Applicant | Boston Scientific Corporation |
| Product code | NPT |
| Received date | Mar 27, 2020 |
| Decision date | Jun 17, 2020 |
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: