PMA supplement
P970051 S112: INTRODUCTION CP900 SERIES RECHARGEABLE BATTERIES (A29 AND A30)
FDA PMA supplement · Real-Time Process · Cochlear Americas
Key facts
| Original PMA | P970051 |
|---|---|
| Supplement number | S112 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | INTRODUCTION CP900 SERIES RECHARGEABLE BATTERIES (A29 AND A30) |
| Generic name | Implant, cochlear |
| Applicant | Cochlear Americas |
| Product code | MCM |
| Received date | Sep 26, 2013 |
| Decision date | Dec 20, 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: