News | Peripheral Artery Disease (PAD) | November 10, 2023

Getinge Announces U.S. Commercial Availability of iCast Covered Stent System for Treatment of Iliac Arterial Occlusive Disease

Getinge announced commercial availability of the iCast covered stent system in the United States

November 10, 2023 —Getinge announced commercial availability of the iCast covered stent system in the United States for the treatment of iliac arterial occlusive disease. In March 2023, the iCast covered stent received premarket approval from the U.S. Food and Drug Administration (FDA) for the treatment of iliac arterial occlusive disease. Lower extremity peripheral artery disease (PAD) is estimated to affect approximately 8.5 million people in the U.S. per year [1],[2]

“We are very pleased that the iCast covered stent is now available to clinicians and hospital systems throughout the U.S. for the treatment of this serious and often painful condition for patients,” said Patricia Fitch, President Getinge, North America. “This indication is another reflection of Getinge’s commitment to bringing our U.S. customers the high-quality products and support they need for their patients.” 

To support the commercial availability of the iCast covered stent, Getinge will take part in two upcoming medical meetings: 

• Getinge will attend the VIVA (Vascular InterVentional Advances) conference being held October 30-November 1, 2023, at the Wynn Hotel in Las Vegas, Nevada. Attendees will be able to access information about the iCast covered stent at the Getinge booth (#316) during the conference. Getinge will also sponsor a breakout session led by Christopher J. Smolock, MD, Vascular Surgeon at Mount Sinai Queens, titled “Effective Treatment of TASC D Common Iliac Lesions Utilizing the iCast Covered Stent System” during the meeting. Dr. Smolock’s presentation will be held Wednesday, November 1, 2023, from 10:20am-10:45am PST in the Red Theater (Lafite Ballroom). 

• Getinge will also attend the VEITH symposium being held November 14-18, 2023, at the Hilton Midtown Hotel in New York, New York. Attendees can access information about the iCast covered stent at the Getinge booth (#513) and also attend a satellite symposium on Thursday, November 16 from 4:00pm to 6:00pm EST.  

“iCast, marketed outside the U.S. as Advanta V12, has been used by clinicians for more than 20 years. The use of iCast for the treatment of iliac arterial occlusive disease builds on this strong history of clinical experience and reflects Getinge’s commitment to developing and delivering products that represent the highest standards in safety and performance,” said Therese Mueller, Vice President of Sales, Acute Care Therapies at Getinge. "We are very pleased that the system and the full range of Getinge support materials and services will now be available to support physicians who treat patients affected by this devastating disease." 

For more information: www.getinge.com 

 

Sources 

[1] Neisen, M. J. (2009). Endovascular management of aortoiliac occlusive disease. Seminars in Interventional Radiology, 26(4), 296–302. https://doi.org/10.1055/s-0029-1242199 

[2] Gerhard-Herman MD, Gornik HL, Barrett C, Barshes NR, Corriere MA, Drachman DE, Fleisher LA, Fowkes FGR, Hamburg NM, Kinlay S, et al. (2017). 2016 AHA/ACC guideline on the management of patients with lower extremity peripheral artery disease: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation, 135, e686–e725. doi: 10.1161/CIR.000000000000047


Related Content

News | FDA

June 18, 2024 — Elixir Medical has announced the company’s novel bioadaptive implant, DynamX Sirolimus-Eluting Coronary ...

Home June 18, 2024
Home
News | FDA

June 17, 2024 — Elutia Inc., a pioneer in drug-eluting biomatrix products, today announced that its Antibiotic-Eluting ...

Home June 17, 2024
Home
News | FDA

June 13, 2024 — Xeltis, a leading developer of transformative implants that enable the natural creation of living and ...

Home June 13, 2024
Home
News | FDA

June 3, 2024 — Heuron, a specialized medical AI startup focused on brain and neurological disorders based in South Korea ...

Home June 03, 2024
Home
News | FDA

May 17, 2024 — Implicity, a leader in remote patient monitoring and cardiac data management solutions, announced it has ...

Home May 17, 2024
Home
News | FDA

May 15, 2024 — The U.S. Food and Drug Administration (FDA) announced that Abbott is recalling the HeartMate 3 LVAS by ...

Home May 15, 2024
Home
News | FDA

May 8, 2024 — The US Food and Drug Administration (FDA) is alerting health care providers and facilities about our ...

Home May 08, 2024
Home
News | FDA

May 8, 2024 — 4C Medical Technologies, Inc. ("4C Medical"), a medical device company dedicated to advancing minimally ...

Home May 08, 2024
Home
News | FDA

May 7, 2024 — RapidAI, the global leader in developing clinically deep Artificial Intelligence (AI) and technology ...

Home May 07, 2024
Home
News | FDA

April 25, 2024 — Provisio Medical announced FDA 510(k) clearance of the Provisio SLT IVUS System. Sonic Lumen Tomography ...

Home April 25, 2024
Home
Subscribe Now