PMA supplement
P870036 S016: MEDTRONIC(R) CORONARY BALLOON DILITATION CATHETERS
FDA PMA supplement · Normal 180 Day Track · Medtronics Interventional Vascular
Key facts
| Original PMA | P870036 |
|---|---|
| Supplement number | S016 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | MEDTRONIC(R) CORONARY BALLOON DILITATION CATHETERS |
| Generic name | Catheters, transluminal coronary angioplasty, percutaneous |
| Applicant | Medtronics Interventional Vascular |
| Product code | LOX |
| Received date | Jan 15, 1992 |
| Decision date | Aug 3, 1992 |
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: