CDRH’s ophthalmic devices advisory panel will look at the evidence supporting PMA approval of Alcon Laboratories Inc.’s AcrySof IQ Restor multifocal toric posterior chamber intraocular lens at a public meeting on Nov. 14, according to an FDA notice.
The company is seeking an indication for the IOL for primary implantation to correct aphakia and astigmatism in patients who...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?