PMA supplement
P800040 S001: CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,
FDA PMA supplement · Cordis Corp.
Key facts
| Original PMA | P800040 |
|---|---|
| Supplement number | S001 |
| Trade name | CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A, |
| Generic name | Stimulator, spinal-cord, totally implanted for pain relief |
| Applicant | Cordis Corp. |
| Product code | LGW |
| Received date | Jun 23, 1981 |
| Decision date | Oct 26, 1981 |
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: