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Nonthermal cyanoacrylate ablation for treatment of superficial venous disease. The VenaSeal™ closure system is safe and effective and backed by long-term data.1-4 Plus, simple innovations and new techniques mean greater* impact for you and your practice.
*All statements of being “greater” are as compared to previous version and procedure technique.
The Abre™ venous self-expanding stent system is designed for the unique challenges of venous disease. It offers easy deployment, to let physicians focus on their patient, and delivers demonstrated endurance, to give patients freedom of movement.5,6
The cusp overlap technique brings precision and control to the TAVR procedure by isolating the non-coronary cusp, providing an accurate anatomical view to access and achieve the target implant depth. In combination with slow deployment starting at the supra-annular level, the valve is able to descend to its target position with minimal catheter manipulation, minimizing the risk of interaction with the conduction system.
Endurant™ AAA stent graft demonstrates consistent and high sac regression rates across straightforward and complex anatomies.7,8 With:
The Onyx ONE Clear Analysis evaluated over 1,500 complex high bleeding risk (HBR) patients, which led Resolute Onyx™ DES to receive an indication for HBR patients and 1-month DAPT labeling.10
Resolute Onyx DES now offers greater expansion capabilities to treat vessel sizes from 2.00–5.00 mm, with the ability to expand XLV sizes up to 6.00 mm.10
The ABRE clinical study demonstrates the safety and effectiveness of the Abre venous stent.5 Learn more about the study and the 12-month results.
The Evolut TAV's supra-annular, self-expanding valve design delivers exceptional hemodynamics and is the only TAVR device to demonstrate hemodynamic superiority in a low-risk clinical trial versus SAVR at one year.13
Read the Circulation: Cardiovascular Interventions article, evaluating Resolute Onyx DES in ~1,500 highly complex HBR patients on 1-month DAPT.
Designed to evaluate if a targeted procedural approach in the distal main and first order branches provides similar BP reductions as those observed in the SPYRAL HTN-OFF MED Pivotal Trial. Learn more at clinicaltrials.gov.
Contact us to learn more and discuss patient eligibility requirements for SPYRAL HTN-ON MED or SPYRAL DYSTAL trials.
Designed to determine the safety and efficacy of renal denervation (RDN) in the presence of up to three standard antihypertensive medications. Learn more at clinicaltrials.gov.
†CAUTION: Investigational device. Limited by federal (U.S.) law to investigational use.
Browse CTO PCI course modules, including physician-narrated videos now available on Medtronic Academy. Log in to start the courses or bookmark for later.
Access interactive global webcasts delivered by industry-leading experts on a wide range of relevant topics related to transcatheter aortic valve replacement.
Watch as subject matter experts review case studies and discuss the most recent clinical evidence, as well as decision-making for complex HBR patients, like those studied in the Onyx ONE Month DAPT Program.
Watch the full, four-part webinar series, “Building Success in CTO PCI — What Would You Do?” including the final segment featuring Dr. Pershad, Dr. Brilakis, Dr. Maran, and Dr. Yeh.
As your partner in the evolving healthcare landscape, we've developed various webinar series for real-time and on-demand learning with peer-to-peer discussion.
Morrison N, Gibson K, Vasquez M, et al. Five-year extension study of patients from a randomized clinical trial (VeClose) comparing cyanoacrylate closure versus radiofrequency ablation for the treatment of incompetent great saphenous veins. J Vasc Surg Venous Lymphat Disord. March 2020;8(6):978-989.
Morrison N, Gibson K, McEnroe S, et al. Randomized trial comparing cyanoacrylate embolization and radiofrequency ablation for incompetent great saphenous veins (VeClose). J Vasc Surg. April 2015;61(4):985-994.
Proebstle T, Alm J, Dimitri S, et al. Three-year follow-up results of the prospective European Multicenter Cohort Study on Cyanoacrylate Embolization for treatment of refluxing great saphenous veins. J Vasc Surg Venous Lymphat Disord. March 2021;9(2):329-334.
Almeida JI, Javier JJ, Mackay EG, Bautista C, Cher DJ, Proebstle TM. Thirty-sixth-month follow-up of first-in-human use of cyanoacrylate adhesive for treatment of saphenous vein incompetence. J Vasc Surg Venous Lymphat Disord. September 2017;5(5):658-666.
ABRE CSR v1.2 30/JUL/2020.
Test data on file at Medtronic. Bench test results may not be indicative of clinical performance.
Bӧckler D, Li C, Dansey K, et al. Sac regression is associated with lower all-cause mortality after contemporary endovascular aneurysm repair — a new paradigm for success. Presented online at ESVS 34th Annual Meeting, October 6, 2020.
Medtronic data on file.
Wakefield TW, Shulkin BL, Fellows EP, Petry NA, Spaulding SA, Stanley JC. Platelet reactivity in human aortic grafts: a prospective, randomized midterm study of platelet adherence and release products in Dacron and polytetrafluoroethylene conduits. J Vasc Surg. February 1989;9(2):234-243.
Resolute Onyx DES IFU.
Holden A. Presented at Charing Cross 2021.
Trerotola SO, Saad TF, Roy-Chaudhury P. Lutonix AV Clinical Trial Investigators. The Lutonix AV Randomized Trial of Paclitaxel-Coated Balloons in Arteriovenous Fistula Stenosis: 2-Year Results and Subgroup Analysis. J Vasc Interv Radiol. January 2020;31(1):1-14.e5.
Popma JJ, Deeb GM, Yakubov SJ, et al. Transcatheter Aortic-Valve Replacement with a Self-Expanding Valve in Low-Risk Patients. N Engl J Med. May 2, 2019;380(18):1706-1715.