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Clinical Studies

LEADER	First In Man (FIM) feasibility study designed to evaluate safety and debris removal performance of the PROTEUS device in diseased Superficial Femoral Arteries (SFA) Reference: EuroPCR 2008, Barcelona
MC-LEADER	Multi- center study designed to evaluate safety and efficacy of the PROTEUS device during lower extremity Percutaneous Transluminal Angioplasty (PTA) [Study was conducted as part of 510(k) submission] LINK to EVToday covering article Reference: Dieter RS, Nanjundappa A. Embolic capture angioplasty. Endovascular Today 2010; 9(9): 64-7.
PROTEUS™ 5x300mm Catheter Study	Multi-center study designed to confirm safety of PROTEUS 5x300mm device in long femoropopliteal lesions.

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