PMA supplement
P040020 S087: AcrySof IQ PanOptix Trifocal Intraocular Lens and AcrySof IQ PanOptix Toric Trifocal Intraocular Lens
FDA PMA supplement · Panel Track · Alcon Research, Ltd.
Key facts
| Original PMA | P040020 |
|---|---|
| Supplement number | S087 |
| Supplement type | Panel Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | AcrySof IQ PanOptix Trifocal Intraocular Lens and AcrySof IQ PanOptix Toric Trifocal Intraocular Lens |
| Generic name | Lens, multifocal intraocular |
| Applicant | Alcon Research, Ltd. |
| Product code | MFK |
| Received date | Jan 31, 2019 |
| Decision date | Aug 26, 2019 |
| Docket number | 19M-4153 |
| Notice date | Sep 6, 2019 |
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: