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EVOLUT PRO SYSTEM Transcatheter Aortic Valve Replacement (TAVI)

The Evolut™ PRO system combines exceptional valve design and advanced sealing with an excellent safety profile.

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Overview

Meet the Evolut PRO System

The Evolut PRO self-expanding transcatheter aortic valve features a unique valve design with an outer wrap that adds surface area contact between the valve and the native aortic annulus to further advance valve sealing performance.

See how the external tissue wrap on the Evolut PRO TAVI performs.

   

PRODUCT DETAILS

EXCEPTIONAL DESIGN

The Evolut PRO valve features an external tissue wrap added to the proven platform design. These legacy and new design features provide the following sealing mechanisms: 

  • The external wrap increases surface contact with native anatomy, providing advanced sealing.
  • The frame oversizing and cell geometry provide consistent radial force across the treatable annulus range.
Evolut PRO valve with shaded external tissue wrap on white background
Partially deployed Evolut PRO valve in the anatomy

THE HEMODYNAMIC ADVANTAGE OF THE EVOLUT TAVI PLATFORM

The Evolut TAVI platform demonstrates EOAs that are consistently large and may have a benefit for healthier, more active patients.

The supra-annular, self-expanding design of the Evolut PRO system provides a large effective orifice area (EOA).  Benefits of a large EOA may include:

  • Less workload for the ventricle1
  • Fewer instances of prosthesis-patient mismatch (PPM), which has been correlated to improved long-term survival2
  • A large EOA provides improved flow, less resistance, and better long-term durability3

Supra-annular valve design maximizes leaflet coaptation and promotes single-digit gradients and large EOAs.

Topview of the Evolut R Transcatheter Aortic Valve

CONTROL AND ACCESS

Features of the EnVeoTM PRO delivery system allow you to treat more patients and position the valve more accurately.

Broadest annulus range*
More patients have access to the minimally invasive TAVI procedure because of the expanded annulus range.

Evolut PRO valves in sizes

Lowest delivery profile
The EnVeo PRO system retains its outer diameter as it enters the vessel and remains at this diameter as it is advanced to the annulus.

Recapture and reposition
The EnVeo PRO delivery system assists in accurate positioning of the valve. The delivery system features a 1:1 response, thus providing immediate feedback between the deployment knob and the movement of the capsule.

In addition, the EnVeo PRO delivery system provides you the option to recapture and reposition for more accurate placement.

Image of the EnVeo PRO delivery system featuring accurate positioning

RESOURCES

MANUALS AND TECHNICAL GUIDES

Access instructions for use and other technical manuals in the Medtronic Manual Library. Search by the product name (e.g., Evolut) or model number.

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Education & Resources

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*

Broadest annulus range based on CT derived diameters.

Measurement is for TAV-in-SAV only.

Up to 80% deployment. The valve can be partially or fully recaptured up to three times prior to the point of no recapture. Third attempt must be a complete recapture and retrieval from patient.

1

Dahou A, Mahjoub H, Pibarot P. Prosthesis-Patient Mismatch After Aortic Valve Replacement. Curr Treat Options Cardiovasc Med. November 2016;18(11):67.

2

Pibarot P, Dumesnil JG. Prosthesis-patient mismatch: definition, clinical impact, and prevention. Heart. August 2006;92(8);1022-1029.

3

Flameng, W, et al. Prosthesis-Patient Mismatch Predicts Structural Valve Degeneration in Bioprosthetic Heart Valves. Circulation. 2010; 121:2123-2129.

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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