FDA Ophthalmic Devices Panel
This article was originally published in The Gray Sheet
Executive Summary
Premarket approval application for a toric intraocular lens for the visual correction of aphakia is scheduled for consideration on July 23 in Gaithersburg, Maryland. The panel also will discuss and vote on a PMA for an excimer laser for correction of sphere-only hyperopia via photorefractive keratectomy. For more information, contact FDA's advisory committee information hotline at 800/741-8138 and use code 12396