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MEDTRONIC TAVI TRANSCATHETER AORTIC VALVE IMPLANTATION (TAVI)

A PARADIGM SHIFT IN THE MANAGEMENT OF PATIENTS WITH SEVERE AORTIC STENOSIS

Transcatheter aortic valve implantation (TAVI) is a minimally invasive, catheter-based procedure to replace the function of the aortic valve.


A LESS INVASIVE TREATMENT OPTION

TAVI may be an excellent option for certain patients because the prevalence of aortic stenosis and co-morbidities increase the risks associated with surgical aortic valve implantation (SAVI).1 Without intervention, the average symptomatic patient life expectancy is 2 to 5 years.2

 

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Bioprosthetic valve partially expanded

<h2 class="tta__headline h2" style="font-weight: normal;">SYMPTOMATIC SEVERE AORTIC STENOSIS<br><b>INCIDENCE IN WESTERN EUROPE<sup>3</sup></b></h2><h2 style="font-size: 60px;">~350,000</h2>

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PATIENT<br>DIAGNOSIS<br>AND SELECTION

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TAVI THERAPY

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1

Schwartz F, et al. The effect of aortic valve replacement on survival Circulation. 1982:66:1105-1110.

2

Lester SJ, Heilbron B, Gin K, et al. The natural history and rate of progression of aortic stenosis. Chest 1998; 113:1109-14.

3

Medtronic data on file.

DISCLAIMER

The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s). Please note that the intended use of a product may vary depending on geographical approvals.

See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.

For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI. If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.

Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.

Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable). For any further information, contact your local Medtronic representative.

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