PMA supplement
P970051 S192: Nucleus 24 Cochlear Implant System (EA22 Stiffener)
FDA PMA supplement · 30-Day Notice · Cochlear Americas
Key facts
| Original PMA | P970051 |
|---|---|
| Supplement number | S192 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Nucleus 24 Cochlear Implant System (EA22 Stiffener) |
| Generic name | Implant, cochlear |
| Applicant | Cochlear Americas |
| Product code | MCM |
| Received date | Sep 9, 2019 |
| Decision date | Oct 8, 2019 |
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: