PMA supplement
P130016 S030: Nucleus Hybrid Implant System
FDA PMA supplement · Real-Time Process · Cochlear Americas
Key facts
| Original PMA | P130016 |
|---|---|
| Supplement number | S030 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | Nucleus Hybrid Implant System |
| Generic name | Cochlear implant with combined electrical stimulation and acoustic amplification |
| Applicant | Cochlear Americas |
| Product code | PGQ |
| Received date | Jun 21, 2017 |
| Decision date | Sep 20, 2017 |
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: