Anteris Technologies hails FDA early feasibility study approval for DurAVR™ | News Direct

Anteris Technologies hails FDA early feasibility study approval for DurAVR™

Anteris Technologies Ltd
Digital Asset Direct by Anteris Technologies Ltd

facebook icon linkedin icon twitter icon pinterest icon email icon Melbourne, Victoria | December 06, 2022 01:00 PM Eastern Standard Time

Anteris Technologies Ltd (ASX:AVR, OTC:AMEUF) CEO Wayne Paterson discusses with Proactive the news that the US Food and Drug Administration (FDA) has conditionally approved the DurAVR™ transcatheter heart valve (THV) system for investigational device exemption (IDE) application to kick off an early feasibility study (EFS). The study will evaluate the safety and feasibility of the DurAVR™ THV System in the treatment of subjects with symptomatic severe native aortic stenosis.

 

Contact Details

 

Proactive Investors

 

Jonathan Jackson

 

+61 413 713 744

 

Jonathan@proactiveinvestors.com

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