PMA supplement
P930039 S006: SUREFIX TM MODEL 5072 LEAD
FDA PMA supplement · Medtronic, Inc.
Key facts
| Original PMA | P930039 |
|---|---|
| Supplement number | S006 |
| Trade name | SUREFIX TM MODEL 5072 LEAD |
| Generic name | Permanent pacemaker Electrode |
| Applicant | Medtronic, Inc. |
| Product code | DTB |
| Received date | Apr 20, 1998 |
| Decision date | Aug 12, 1998 |
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: