PMA supplement
P900070 S020: MODEL 1256D META MV CARDIAC PULSE GENERATOR
FDA PMA supplement · Real-Time Process · St. Jude Medical, Cardiac Rhythm Management Divisi
Key facts
| Original PMA | P900070 |
|---|---|
| Supplement number | S020 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | MODEL 1256D META MV CARDIAC PULSE GENERATOR |
| Generic name | Implantable pacemaker Pulse-generator |
| Applicant | St. Jude Medical, Cardiac Rhythm Management Divisi |
| Product code | DXY |
| Received date | Sep 10, 1997 |
| Decision date | Oct 7, 1997 |
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: