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IDEV is leading the way in developing minimally invasive medical technologies to protect and preserve anatomical function.
IDEV is focused on products that are truly differentiated and deliver clear patient benefits.
IDEV is investing in research and development.
IDEV. Architects of Intervention.
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IDEV has completed enrollment in the SUPERB (Comparison of the SUPERA PERipheral System to a Performance Goal Derived from Balloon Angioplasty Clinical Trials in the Superficial Femoral Artery) IDE trial to evaluate SUPERA in treating patients with obstructive superficial femoral artery (SFA) disease. SUPERB is a multicenter, prospective, non-randomized, single-arm study enrolling 258 patients at up to 50 sites. The primary efficacy endpoint is patency greater than 66% at 12 months, defined as freedom from restenosis (measured by duplex ultrasound) and TVR. The principal investigators leading this study are nationally respected clinicians, Kenneth Rosenfield, M.D. of Massachusetts General Hospital and Lawrence A. Garcia, M.D. of Caritas St. Elizabeth's Medical Center. For more information visit the SUPERB Study website, or click on the link below for the SUPERB Study Guide
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SUPERA® is a different
class of stent. |
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