PMA supplement
P020030 S004: STELID II, STELIX, AND STLIX II STEROID-ELUTING PACING LEADS
FDA PMA supplement · 135 Review Track For 30-Day Notice · MicroPort CRM S.r.l.
Key facts
| Original PMA | P020030 |
|---|---|
| Supplement number | S004 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | STELID II, STELIX, AND STLIX II STEROID-ELUTING PACING LEADS |
| Generic name | Permanent defibrillator electrodes |
| Applicant | MicroPort CRM S.r.l. |
| Product code | NVY |
| Received date | Oct 11, 2007 |
| Decision date | Oct 17, 2008 |
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: