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FDA approves first retinal implant for adults with advanced retinitis pigmentosa

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On Feb. 20, 2013, the U.S. Food and Drug Administration (FDA) approved the Argus II Retinal Prosthesis System, the first implanted device to treat adult patients with advanced retinitis pigmentosa. The device, which includes a small video camera, a transmitter mounted on a pair of eyeglasses, a video processing unit, and an implanted retinal prosthesis, may improve a patient’s ability to perceive images and movement. Read more.

The views and opinions expressed here are those of the author and do not necessarily reflect the opinions or recommendations of the American Nurses Association, the Editorial Advisory Board members, or the Publisher, Editors and staff of American Nurse Journal. This has not been peer reviewed.

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