PMA supplement
P030004 S022: Onyx Liquid Embolic System and Apollo Onyx Delivery Micro Catheter
FDA PMA supplement · 30-Day Notice · Ev3 Neurovascular
Key facts
| Original PMA | P030004 |
|---|---|
| Supplement number | S022 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Onyx Liquid Embolic System and Apollo Onyx Delivery Micro Catheter |
| Generic name | Agent, injectable, embolic |
| Applicant | Ev3 Neurovascular |
| Product code | MFE |
| Received date | Nov 21, 2019 |
| Decision date | Dec 19, 2019 |
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: