PMA supplement
P820018 S064: REFLEX MODEL 8223E
FDA PMA supplement · Special (Immediate Track) · St. Jude Medical, Inc.
Key facts
| Original PMA | P820018 |
|---|---|
| Supplement number | S064 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | REFLEX MODEL 8223E |
| Generic name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | St. Jude Medical, Inc. |
| Product code | LWP |
| Received date | Jul 18, 1994 |
| Decision date | Aug 30, 1994 |
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: