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Onyx Frontier is the only drug-eluting stent (DES) approved for use in non-LM bifurcation lesions using the provisional stenting technique. See how Onyx Frontier DES is optimized for bifurcation.
A re-engineered delivery system for more flexibility and control. Enhanced visualization for more precise, predictable deployment.
Performance as compared to Evolut™ PRO+ system in bench testing. Bench testing may not be indicative of clinical performance.
Treat more diseased vein — maximize your impact. The VenaSeal closure system delivers immediate and lasting vein closure with its proprietary medical adhesive formula, with a demonstrated 94.6% closure rate at five years.1–5
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.6,7
Only CoreValve™/Evolut TAVR has shown a durability benefit over SAVR in multi-centered, randomized clinical trials out to 5 years8 and 10 years.9
EndoSuture Aneurysm Repair (ESAR) with the Heli-FX™ EndoAnchor™ system is your defense for patients at risk for suboptimal outcomes.
Our co-promotion agreement with CathWorks adds the CathWorks FFRangio®* System to our PCI portfolio. See how the technology's use of advanced artificial intelligence and computational science can help inform treatment decisions.
Designed for end-stage renal disease (ESRD) patients requiring hemodialysis, the Ellipsys™ system is a unique single-catheter, nonsurgical option for physicians to create an arteriovenous (AV) fistula, a traditionally invasive procedure that — until the advent of percutaneous AVF technology — had not changed in more than 50 years.
The IN.PACT AV Access Study demonstrates the safety and effectiveness of the IN.PACT™ AV drug-coated balloon in arteriovenous fistulas.15 Learn more about the study and the 36-month results.
The ABRE clinical study demonstrates the safety and effectiveness of the Abre venous stent.6 Learn more about the study and the 36-month results.
Designed to evaluate the long-term safety, efficacy, and durability of renal denervation in real-world patients with uncontrolled hypertension and associated comorbidities.
Caution: Investigational device. Limited by federal (U.S.) law to investigational use.
Evolut™ TAVR shows outstanding outcomes in low risk patients over time.16
ESAR reinforces and protects the proximal seal, leading to better outcomes in wide necks. View data on wide necks from literature compared to the three-year wide neck results from the ANCHOR Registry.
The VenaSeal Spectrum Program is the largest post-market clinical study of the VenaSeal closure system compared to the current standards of care.
Coronary Corner can now be found on Medtronic Academy 2.0, the latest version of our web-based education platform. Find all the same great resources on the enhanced site now.
This seven-part webinar series hosted by HTN clinical experts delves into several aspects of patient care, including diagnosis and treatment, establishing a care pathway, and addressing health equity.
Explore our new aortic stenosis and TAVR-related resources that will help you build your knowledge and support your patient education efforts in your heart valve clinic.
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.
Visit Medtronic Academy to browse our latest resources, including step-by-step procedural videos of non-left main bifurcation using the provisional stenting technique.
Access a wide range of interactive courses, case studies, presentations, images, and videos from your phone, tablet, or desktop.
Visit Medtronic Academy®Third-party brands are trademarks of their respective owners.
TAVR risks may include, but are not limited to: death, stroke, damage to the arteries, bleeding, and the need for a permanent pacemaker.
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.
Gibson K, Ferris B. Cyanoacrylate closure of incompetent great, small and accessory saphenous veins without the use of post-procedure compression: Initial outcomes of a post-market evaluation of the VenaSeal System (the WAVES Study). Vascular. April 2017;25(2):149–156.
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.
Morrison N, Gibson K, Vasquez M, Weiss R, Jones A. 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. November 2020;8(6):978–989.
Abre stent Instructions for Use.
Test data on file at Medtronic. Bench test results may not be indicative of clinical performance.
O'Hair D, Yakubov SJ, Grubb KJ, et al. Structural valve deterioration after self-expanding transcatheter or surgical aortic valve implantation in patients at intermediate or high risk. JAMA Cardiol. February 1, 2023;8(2):111–119.
Jørgensen T. Ten-year follow-up after transcatheter or surgical aortic valve implantation in severe aortic valve stenosis. Presented at ESC Congress; August 2023.
Melas N, Perdikides T, Saratzis A, Saratzis N, Kiskinis D, Deaton DH. Helical EndoStaples enhance endograft fixation in an experimental model using human cadaveric aortas. J Vasc Surg. June 2012;55(6):1726–1733.
Schlösser FJV, de Vries JPPM, Chaudhuri A. Is it Time to Insert EndoAnchors into Routine EVAR? Eur J Vasc Endovasc Surg. April 2017;53(4):458–459.
Tassiopoulos AK, Monastiriotis S, Jordan WD, Muhs BE, Ouriel K, De Vries JP. Predictors of early aortic neck dilatation after endovascular aneurysm repair with EndoAnchors. J Vasc Surg. July 2017;66(1):45–52.
ANCHOR 4-year primary arm. 2019 data cut. Medtronic data on file.
Muhs BE, Jordan W, Ouriel K, Rajaee S, de Vries JP. Matched cohort comparison of endovascular abdominal aortic aneurysm repair with and without EndoAnchors. J Vasc Surg. June 2018;67(6):1699–1707.
Holden A. The IN.PACT AV Access Study: Results through 36 Months. Presented at Charing Cross 2022.
Forrest JK, Deeb GM, Yakubov SJ, et al. Evolut Low Risk Trial Investigators. 4-Year Outcomes of Patients With Aortic Stenosis in the Evolut Low Risk Trial. J Am Coll Cardiol. November 28, 2023;82(22):2163-2165.