PMA supplement
P930014 S017: ACRYSOF IQ MODEL SN60WF POSTERIOR CHAMBER INTRAOCULAR LENS
FDA PMA supplement · Normal 180 Day Track · Alcon Laboratories, Inc.
Key facts
| Original PMA | P930014 |
|---|---|
| Supplement number | S017 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | ACRYSOF IQ MODEL SN60WF POSTERIOR CHAMBER INTRAOCULAR LENS |
| Generic name | Intraocular lens |
| Applicant | Alcon Laboratories, Inc. |
| Product code | HQL |
| Received date | Mar 2, 2006 |
| Decision date | Apr 27, 2007 |
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: