PMA supplement
P890003 S063: 9767/9767L PROGRAMMING HEAD AND MODEL9990 DESKTOP SOFTWARE
FDA PMA supplement · Normal 180 Day Track · Medtronic, Inc.
Key facts
| Original PMA | P890003 |
|---|---|
| Supplement number | S063 |
| Supplement type | Normal 180 Day Track |
| Trade name | 9767/9767L PROGRAMMING HEAD AND MODEL9990 DESKTOP SOFTWARE |
| Generic name | Implantable pacemaker Pulse-generator |
| Applicant | Medtronic, Inc. |
| Product code | DXY |
| Received date | Apr 11, 2001 |
| Decision date | May 7, 2001 |
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: