Pixium Vision SA Receives FDA Approval to Begin Human Clinical Study of Its Prima Sub-Retinal Implant in the US
January 04, 2018 at 01:00 am
Pixium Vision announced that it has received the approval from the US Food and Drug Administration (FDA) to begin the clinical feasibility study for PRIMA, Pixium Vision's new-generation miniaturized wireless photovoltaic sub-retinal implant, in patients with Atrophic Dry Age-related Macular Degeneration (AMD). This first approval in the US will allow Pixium Vision to commence a feasibility study of the PRIMA device and follows a thorough review by the FDA.