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Medigus Ltd receives FDA clearance for next generation MUSE system

Sunday, 23 Mar 2014 04:03am EDT 

Medigus Ltd:Says that United States Food and Drug Administration (FDA) has granted 510(k) clearance for next generation MUSE system, formerly known as the SRS system.MUSE is a device which enables an incisionless procedure by performing an anterior partial fundoplication with standard surgical staples in a less invasive way.Procedure currently targets patients with symptomatic chronic gastroesophageal reflux disease (GERD.MUSE system provides these patients, who are typically at higher risk of developing esophageal cancer, with potential long-term solution which aims to restore the esophageal anatomy with minimally invasive tool in order to reduce or eliminate their GERD symptoms. 

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-1.5 -3.13%
22 Sep 2014