PMA supplement
P800041 S007: ENDOCARDIAL PACEMAKER LEAD W/CARBON TIP
FDA PMA supplement · Normal 180 Day Track · Pacesetter Systems
Key facts
| Original PMA | P800041 |
|---|---|
| Supplement number | S007 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | ENDOCARDIAL PACEMAKER LEAD W/CARBON TIP |
| Generic name | Permanent pacemaker Electrode |
| Applicant | Pacesetter Systems |
| Product code | DTB |
| Received date | Jan 9, 1987 |
| Decision date | Jun 22, 1987 |
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: