PMA supplement
P010023 S002: MAXUM SYSTEM
FDA PMA supplement · Normal 180 Day Track No User Fee · Ototronix, LLC
Key facts
| Original PMA | P010023 |
|---|---|
| Supplement number | S002 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | MAXUM SYSTEM |
| Generic name | Implant, hearing, active, middle ear, partially implanted |
| Applicant | Ototronix, LLC |
| Product code | MPV |
| Received date | Aug 19, 2009 |
| Decision date | Oct 8, 2009 |
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: