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Ivantis sends premarket approval submission for Hydrus microstent to FDA

17:30 EST 8 Nov 2017 | Healio

Ivantis has submitted a final premarket approval module to the FDA for its Hydrus microstent to lower IOP in open-angle glaucoma, according to a company press release.
The submission included data from the prospective, randomized HORIZON pivotal trial, in which 556 patients at 38 centers in nine countries received the MIGS device with cataract surgery or cataract surgery alone and were followed for 2 years.
The Hydrus is the size of an eyelash and is placed in Schlemm’s canal using a minimally invasive microsurgical procedure, the release said.
“The submission of Ivantis’ PMA

Original Article: Ivantis sends premarket approval submission for Hydrus microstent to FDA

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