Covidien has completed patient enrollment in its VISIBILITY and DURABILITY Iliac stent clinical study series. The prospective, multinational, multicenter studies, which have enrolled 150 patients from 23 centers in the US and Europe, are ...
Cordis has obtained regulatory approval from the US Food and Drug Administration (FDA) to use its S.M.A.R.T. CONTROL Vascular Stent systems in the superficial femoral artery (SFA) and/or the proximal popliteal artery (PPA). The Stent ...
Tags: FDA, Stent systems, proximal popliteal artery, superficial femoral artery
Svelte Medical Systems has commenced First Assessment of the Acrobat Stenting Technique European Post-Market Registry (FAASTER) study. The multi-center registry study, which will enroll up to 1,500 patients, is designed to evaluate the ...
Tags: Svelte Medical Systems, FAASTER, FAASTER study, registry study
Flexible Stenting Solutions has received CE mark approval for its FlexSten Iliac Self Expanding Stent system for the treatment of symptomatic atherosclerotic disease of the common and/or external iliac arteries. The FlexStent Iliac Stent ...
Tags: Flexible Stenting Solutions, FlexSten Iliac Self Expanding Stent system