PMA supplement
P020050 S023: WAVELIGHT EX500 EXCIMER LASER SYSTEM, ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM
FDA PMA supplement · Panel Track · Alcon Laboratories, Inc.
Key facts
| Original PMA | P020050 |
|---|---|
| Supplement number | S023 |
| Supplement type | Panel Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | WAVELIGHT EX500 EXCIMER LASER SYSTEM, ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM |
| Generic name | Excimer laser system |
| Applicant | Alcon Laboratories, Inc. |
| Product code | LZS |
| Received date | Jul 20, 2015 |
| Decision date | Nov 21, 2016 |
| Docket number | 16M-4046 |
| Notice date | Nov 30, 2016 |
At a glance
- No Expedited review granted
- Yes Approval order on file
- Yes 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: