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Transcatheter aortic valve implantation (TAVi)

Procedure and performance

From the design to the procedure, the Evolut™ TAVI platform was developed to help you get your patients back to their active lifestyles.

The Evolut™ TAVI advantage

Our valve is designed to drive favorable patient outcomes through procedural excellence and sustained hemodynamics over time. 

Evolut FX transcatheter aortic valve being deployed using the Evolut TAVR/TAVI implant procedure

Precision and control

Specifically developed to enhance procedural consistency, the Evolut™ TAVI implant procedure with cusp overlap technique facilitates implant depth accuracy1 and predictable valve deployment. Additional procedural techniques such as flush port at 3 o'clock help to achieve commissural alignment that may facilitate future coronary access.2

Coronary access

Future coronary access is feasible with the Evolut™ platform. See how you can keep future treatment options open by leveraging the design of the valve frame and following our procedural techniques.2

Evolut transcatheter aortic valve with catheter accessing the coronary

Durability starts with design

The Evolut™ TAVI platform is built on the original CoreValve™ platform, which pioneered the design elements that enable excellent hemodynamic performance. See how we designed for durability.

References

1

Grubb KJ, Gada H, Mittal S, et al. Clinical Impact of Standardized TAVR Technique and Care Pathway: Insights From the Optimize PRO Study. JACC Cardiovasc Interv. March 13, 2023;16(5):558–570.

2

Tang GHL, Zaid S, Fuchs A, et al. Alignment of Transcatheter Aortic-Valve Neo-Commissures (ALIGN TAVR): Impact on Final Valve Orientation and Coronary Artery Overlap. JACC Cardiovasc Interv. May 11, 2020;13(9):1030–1042.

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.

For any further information, contact your local Medtronic representative.

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