PMA supplement
P960009 S008: ACTIVA TREMOR CONTROL THERAPY SYSTEM
FDA PMA supplement · Normal 180 Day Track · Medtronic, Inc.
Key facts
| Original PMA | P960009 |
|---|---|
| Supplement number | S008 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | ACTIVA TREMOR CONTROL THERAPY SYSTEM |
| Generic name | Stimulator, electrical, implanted, for parkinsonian tremor |
| Applicant | Medtronic, Inc. |
| Product code | MHY |
| Received date | Oct 28, 1999 |
| Decision date | Dec 17, 1999 |
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: