202
Participants
Start Date
August 31, 2007
Primary Completion Date
June 30, 2010
Study Completion Date
December 31, 2012
Herculink Elite Renal Stent System
This is a prospective, non-randomized, single arm, multi-center study to evaluate the safety and effectiveness of the RX Herculink Elite Renal Stent System in patients with sub-optimal renal PTA results in de novo or restenotic renal artery lesions. Patients who satisfy the inclusion/exclusion criteria will be enrolled at sites in the United States. Patients will have follow up visits for evaluation.
Abbott Vascular, Santa Clara
Lead Sponsor
Abbott Medical Devices
INDUSTRY