, extracts from the annual report issued few weeks ago.
“Continued preparations to initiate the DurAVR® Transcatheter Heart Valve’s (“THV”) randomized global pivotal study (the “Pivotal Trial”) – request for Investigational Device Exemption (“IDE”) on track for submission to the U.S. Food and Drug Administration (“FDA”) in the first quarter of 2025.”
Next couple of weeks are going to be very interesting.
Not Advice, DYOR
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