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Evolut™ FX+ System for transcatheter aortic valve implantation (TAVI)

The Evolut™ FX+ transcatheter aortic valve system is designed with specific features intended to enable lifetime management solutions such as coronary access.

 

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Evolut FX+ product

Overview

Evolut FX+ System

Explore the Evolut™ FX+ system

Built on the original CoreValve™ platform, the Evolut™ FX+ valve is engineered with specific design elements to enable coronary access and promote sustained valve performance over time.1,2

Performance as compared to Evolut™ PRO+ and FX system in bench testing. Bench testing may not be indicative of clinical performance.

Product details

Built for durability

Designed to maintain the same radial force at the inflow and structural strength at the outflow as the Evolut™ FX valve.1

 

Designed for access

Designed with three windows that are 4 times larger to enable lifetime management solutions such as coronary access.2

Performance as compared to Evolut™ PRO+ and FX system in bench testing. Bench testing may not be indicative of clinical performance.

Evolut fxplus 23 prll

Manuals and technical guides

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

Resources


Contact us

Sign up to learn more about Evolut™ FX, and one of our team members will be in touch with you.

Email: rs.structuralheartinfo@medtronic.com


EvolutTM TAVI in action

Explore our valve design and the performance of the Evolut™ platform over time.

1

Based on Evolut™ FX+ Test Reports: D01073856, D01095344, D01084996. Medtronic data on file. Performance as compared to Evolut™ PRO+ and FX system in bench testing. Bench testing may not be indicative of clinical performance.  

2

Based on Evolut™ FX+ Test Report: DO1106198 Rev. A. Medtronic computational data model on file compared to the Evolut™ platform. Bench top computational model may not be indicative of clinical performance.  

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.

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