PMA supplement
P040044 S001: MYNX VASCULAR CLOSURE DEVICE
FDA PMA supplement · Panel Track · Cordis US Corporation
Key facts
| Original PMA | P040044 |
|---|---|
| Supplement number | S001 |
| Supplement type | Panel Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | MYNX VASCULAR CLOSURE DEVICE |
| Generic name | Device, hemostasis, vascular |
| Applicant | Cordis US Corporation |
| Product code | MGB |
| Received date | Apr 6, 2006 |
| Decision date | May 16, 2007 |
| Docket number | 07M-0285 |
| Notice date | Jul 20, 2007 |
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: