Peripheral

Phoenix atherectomy system

Hybrid atherectomy system

Find similar products

The Phoenix atherectomy system combines the benefits of existing atherectomy systems to deliver a unique, hybrid atherectomy option to help physicians tailor the treatment approach for each patient.¹ It cuts, captures, and clears diseased tissue with one insertion. Phoenix treats a broad range of tissue types, from soft plaque to calcified arteries, and can be used for lesions above and below the knee.²

Specifications

1.8mm x 130cm tracking catheter
1.8mm x 130cm tracking catheter
Part Number
  • P18130K
Introducer size
  • 5F (<gt/>1.8 mm)
Working length
  • 130 cm
Guidewire diameter
  • 0.014”
1.8mm x 149cm tracking catheter
1.8mm x 149cm tracking catheter
Part Number
  • P18149K
Introducer size
  • 5F (<gt/>1.8 mm)
Working length
  • 149 cm
Guidewire diameter
  • 0.014”
2.2mm x 130cm tracking catheter
2.2mm x 130cm tracking catheter
Part Number
  • P22130K
Introducer size
  • 6F (<gt/>2.2 mm)
Working length
  • 130 cm
Guidewire diameter
  • 0.014”
2.2mm x 149cm tracking catheter
2.2mm x 149cm tracking catheter
Part Number
  • P22149K
Introducer size
  • 6F (<gt/>2.2 mm)
Working length
  • 149 cm
Guidewire diameter
  • 0.014”
2.4mm x 127cm deflecting catheter
2.4mm x 127cm deflecting catheter
Part Number
  • PD24127K
Introducer size
  • 7F (<gt/>2.4 mm)
Working length
  • 127 cm
Guidewire diameter
  • 0.014”
  • 1. Hybrid atherectomy refers to the Phoenix family of products. 2.4mm deflecting catheter is the only device with directional cutting ability.
  • 2. Monitor flow of excised material into the disposal reservoir during operation of the Catheter. If flow of excised material ceases during the procedure, this is a sign that the Catheter drive system (cutter, torque shaft, or Handle motor drive) may not be operating properly.
  • 3. Phoenix atherectomy device is indicated for vessels 2.5mm in diameter and above.
  • 4. Endovascular Atherectomy Safety and Effectiveness Study (EASE), ClinicalTrials.gov Identifier NCT01541774 (accessed 23Oct2015). Results presented at the Vascular Interventional Advances (VIVA) Conference in October of 2013 (Las Vegas, NV) by Stephen Williams, MD.
  • 5. Case study results are not predictive. Results in other cases may vary.
  • 6. Case performed by Dr. Christopher LeSar at the Vascular Institute of Chattanooga.
  • 7. Case performed by Dr. Joseph Griffin at Baton Rouge General Hospital.
  • 8. Center mass cutting device when the guidewire is centered.
  • 9. Case performed by Dr. William Crowder in Jackson, Mississippi.
  • 10. Case performed by Dr. Tom Davis in Detroit, MI.