PMA supplement
P960030 S009: PASSIVE PLUS DX, MODELS 1336T, 1342T, 1343K, 1345K, 1346T
FDA PMA supplement · Real-Time Process · ABBOTT MEDICAL
Key facts
| Original PMA | P960030 |
|---|---|
| Supplement number | S009 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | PASSIVE PLUS DX, MODELS 1336T, 1342T, 1343K, 1345K, 1346T |
| Generic name | Permanent pacemaker Electrode |
| Applicant | ABBOTT MEDICAL |
| Product code | DTB |
| Received date | Dec 4, 2002 |
| Decision date | Jan 22, 2003 |
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: