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Unable to tolerate antiplatelet therapy\n* Inability to anticoagulate the patient with heparin, enoxaparin or other parenteral antithrombin, or known to have uncorrected bleeding disorders (e.g., gastro-intestinal ulcer, menorrhagia, liver failure, heparin-induced thrombocytopenia (HIT))\n* Any condition for which, in the opinion of the Investigator, participation would not be in the best interest of the subject (e.g., contraindication to use of Artix per local approved labeling, compromise the well-being or that could prevent, limit, or confound the protocol-specified assessments)\n* Current participation in another drug or device study that, in the investigator's opinion, would interfere with participation in this study","ALL","18 Years",{"count":237,"type":238},250,"ESTIMATED","INTERVENTIONAL",[241],"NA","This study is a post-market, prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the Artix Thrombectomy System in patients with acute lower 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