PMA supplement
P190008 S034: IN.PACT AV Paclitaxel-coated Percutaneous Transluminal Angioplasty Balloon Catheter
FDA PMA supplement · 30-Day Notice · Medtronic Vascular, Inc.
Key facts
| Original PMA | P190008 |
|---|---|
| Supplement number | S034 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | IN.PACT AV Paclitaxel-coated Percutaneous Transluminal Angioplasty Balloon Catheter |
| Generic name | Drug-coated peripheral transluminal angioplasty catheter |
| Applicant | Medtronic Vascular, Inc. |
| Product code | PRC |
| Received date | Oct 10, 2024 |
| Decision date | Oct 21, 2024 |
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: