The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Renal Stent to Treat Renal Artery Stenosis

General Clinical Inclusion Criteria:

- Subject is ≥18 years of age.

- Subject and subject's physician agree to have the subject return for all required
contact following study enrollment.

- Subject has been informed of the nature of the study, and has provided written
informed consent, approved by the appropriate Institutional Review Board (IRB) of
the respective clinical site.

- Subject is a candidate for renal artery stenting.

- Subject has uncontrolled systolic hypertension (systolic Blood Pressure[SBP] ≥140
mmHg), or uncontrolled diastolic hypertension (diastolic BP [DBP] ≥90 mmHg), or a
combination of both in the presence of at least two (2) or more antihypertensive
medications.

- Subject has a baseline serum Creatinine of <2.5mg/dl

Angiographic Inclusion Criteria

- Subject has either unilateral or bilateral de novo or restenotic after Percutaneous
Transluminal Angioplasty (PTA) (in-stent restenosis excluded) atherosclerotic
lesion(s). If bilateral lesions are to be treated, the most severe lesion must be
successfully treated without complications before progressing to treat the second
lesion. Treatment of bilateral lesions is to occur in the same procedural event.

- Renal stenosis must be visually estimated to be ≥60% by angiography.

- Subject has a suboptimal PTA result, defined as one of the following:

- ≥50% residual stenosis

- 10 mm Hg mean gradient or 20 mm Hg peak systolic gradient across the target
lesion

- A flow-limiting dissection (NHLBI grade D) or TIMI flow <3

- Renal stenosis must be visually estimated to be within 10 mm of the aortic renal
border by angiography.

- Target vessel reference diameter must be visually estimated to be ≥4mm and ≤7mm by
angiography

- Target lesion length must be visually estimated to be ≤15mm (including dissection)
by angiography.

- Expected ability to deliver the stent to the lesion (absence of excessive tortuosity
or calcification).

- Expected ability to fully expand the stent.

Clinical Exclusion Criteria

- Subject has known hypersensitivity or contraindication to cobalt chromium or
standard intraprocedure anticoagulant(s); subject has sensitivity to contrast which
cannot be adequately pre-treated with medication.

- Subject has known allergy or contraindication to clopidogrel (Plavix) or aspirin.

- Subject has known bleeding disorder or hypercoagulable disorder, or will refuse
blood transfusions.

- Subject has suffered a gastrointestinal (GI) bleed within 30 days before the index
procedure that would interfere with antiplatelet therapy.

- Subject has renal insufficiency defined as serum Creatinine >2.5 mg/dl.

- Subject has any immunosuppressive disorder, access site infection, or acute systemic
infection due to any cause.

- Subject has other medical illnesses (e.g., cancer, end-stage congestive heart
failure) that may cause the subject to be non-compliant with protocol requirements,
confound the data interpretation, or is associated with a life expectancy of less
than three years.

- Subject has any medical illnesses that would make them unlikely to respond to
treatment (e.g., sickle cell nephropathy/sickle cell disease, scleroderma,
arteriolar nephrosclerosis, hemolytic-uremic syndrome and vasculitis).

- Subject has had a Q-wave MI within 30 days before index procedure.

- Subject has had a stroke or TIA within 30 days before index procedure.

- Subject has a history of congestive heart failure and has a previously documented
LVEF ≤25%.

- Subject is normotensive or has adequate control of hypertension (SBP <140 mmHg and
DBP <90 mm Hg) utilizing diet control and/or medication regimen involving only one
antihypertensive medication.

- Subject has acute thrombophlebitis or deep vein thrombosis.

- Subject is actively participating in another drug or device trial and has not
completed the required protocol follow-up period. Subject may be enrolled only once
in this study (Protocol # 05-102) and may not participate in any other clinical
trial during the follow-up period.

- Subject is unable to understand and cooperate with study procedures or provide
informed consent.

- Subject is unable to return for follow-up visits (distance, etc).

- Subject is pregnant.

- Subject has undergone vascular surgery (CABG, AAA repair, AF bypass) and has not
fully recovered from the effects of surgery (<3 months).

- Subject has planned staged treatment of bilateral renal artery stenosis.

- Subject has had prior surgical intervention to the target artery, or has undergone
previous stent placement in the target lesion.

- Target lesion is located in a transplanted kidney.

- Kidney to be treated is <8 cm as determined by duplex ultrasound report, CTA report,
or MRA report within 180 days before procedure. If kidney size is documented by more
than one method, e.g. CTA and ultrasound, and one of the methods is duplex
ultrasound, the kidney size as documented by duplex ultrasound shall be used to
determine study eligibility.

- Subject has planned additional ancillary procedure(s) during renal stenting
procedure.

Angiographic Exclusion Criteria

- Subject has a lesion segment, including dissection, >15 mm in length.

- Requirement for >1 stent to treat full length of lesion and dissection.

- Target lesion has a total (100%) occlusion.

- Evidence of thrombus or mobile filling defect in the target lesion or vessel.

- Subject has co-existing aneurysmal or occlusive disease of the abdominal aorta
requiring surgical reconstruction during the follow-up period.

- Target lesion is non-atherosclerotic (fibromuscular dysplasia).

- Subject artery has patent bifurcation within 10 mm of ostium that might be covered
by placement of a stent.

- The target lesion is within the artery of a solitary functioning kidney or, the
subject has a contralateral totally occluded renal artery.

- For planned treatment of bilateral lesions: the more critical lesion, i.e. lesion
with the greater stenosis (which should be treated first), is either treated
unsuccessfully or requires a bailout procedure. (NOTE: Less critical lesion is
excluded at this point.)

- Subject has any condition that precludes proper angiographic assessment or makes
percutaneous arterial access unsafe.

- The target lesion is densely calcified and will not yield during balloon dilation.

- Subject has had recent change in renal function after unrelated catheter or surgical
procedure with the clinical stigmata of atheroemboli syndrome (i.e., livedo
reticularis: non-occlusive mesenteric ischemia; digital gangrene; progressive renal
insufficiency without other identifiable etiology).

- Subject has an accessory renal artery that has >50% stenosis. Accessory renal
arteries may not be stented as part of this study.