PMA supplement
P840001 S232: ITREL 4 NEUROSTIMULATOR, ITREL 3 NEUROSTIMULATOR, SYNERGY NEUROSTIMULATOR, SYNERGY VERSITREL NEUROSTIMULATOR
FDA PMA supplement · 30-Day Notice · Medtronic Neuromodulation
Key facts
| Original PMA | P840001 |
|---|---|
| Supplement number | S232 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | ITREL 4 NEUROSTIMULATOR, ITREL 3 NEUROSTIMULATOR, SYNERGY NEUROSTIMULATOR, SYNERGY VERSITREL NEUROSTIMULATOR |
| Generic name | Stimulator, spinal-cord, totally implanted for pain relief |
| Applicant | Medtronic Neuromodulation |
| Product code | LGW |
| Received date | Jan 22, 2013 |
| Decision date | Feb 14, 2013 |
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: