PMA supplement
P840024 S036: IF4 BOARD FOR THE DUAL PROCESSOR INTERFACE SYSTEM
FDA PMA supplement · Normal 180 Day Track · Cochlear Americas
Key facts
| Original PMA | P840024 |
|---|---|
| Supplement number | S036 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | IF4 BOARD FOR THE DUAL PROCESSOR INTERFACE SYSTEM |
| Generic name | Implant, cochlear |
| Applicant | Cochlear Americas |
| Product code | MCM |
| Received date | Nov 15, 1991 |
| Decision date | Sep 14, 1992 |
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: