PMA supplement
P030005 S001: CONTAK RENEWAL TR, MODELS H120, H125
FDA PMA supplement · 30-Day Notice · Guidant Corp.
Key facts
| Original PMA | P030005 |
|---|---|
| Supplement number | S001 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | CONTAK RENEWAL TR, MODELS H120, H125 |
| Generic name | Permanent pacemaker Electrode |
| Applicant | Guidant Corp. |
| Product code | DTB |
| Received date | Feb 4, 2004 |
| Decision date | Mar 3, 2004 |
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: