PMA supplement
P840024 S078: NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM (ADULT)
FDA PMA supplement · 30-Day Notice · Cochlear Americas
Key facts
| Original PMA | P840024 |
|---|---|
| Supplement number | S078 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM (ADULT) |
| Generic name | Implant, cochlear |
| Applicant | Cochlear Americas |
| Product code | MCM |
| Received date | Apr 15, 1999 |
| Decision date | May 7, 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: