PMA supplement
P140031 S205: Edwards Commander Delivery System (9600LDS20; 9600LDS23; 9600LDS26; 9600LDS29; 9750CM20; 9750CM23; 9750CM26; 9750CM29)
FDA PMA supplement · 30-Day Notice · Edwards Lifesciences, LLC
Key facts
| Original PMA | P140031 |
|---|---|
| Supplement number | S205 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Edwards Commander Delivery System (9600LDS20; 9600LDS23; 9600LDS26; 9600LDS29; 9750CM20; 9750CM23; 9750CM26; 9750CM29) |
| Generic name | Aortic valve, prosthesis, percutaneously delivered |
| Applicant | Edwards Lifesciences, LLC |
| Product code | NPT |
| Received date | Jun 5, 2026 |
| Decision date | Jun 30, 2026 |
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: