Evolut™ FX System for transcatheter aortic valve implantation (TAVI)
The Evolut™ FX transcatheter aortic valve system goes beyond your expectations for precision, control, and predictability in TAVI procedures*.
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Overview
Delivering beyond*
Raise your expectations for what is possible with the Evolut™ FX system.
Precision and control*
Smooth, controlled, precise, and predictable.
These are the hallmarks of a successful TAVI procedure — and the inspiration for the Evolut™ FX transcatheter aortic valve system.
Product details
Predictable performance*
Evolut™ FX system enhancements make TAVI procedures easier to visualize and more predictable.
Radiopaque gold markers provide a reference for deployment depth and commissure location.
Optimized stability layer increases catheter support during deployment and provides 53% less ventricular movement*1 so you get greater control when it matters most.
As demonstrated in bench testing.
Re-engineered delivery system expands flexibility for 360° range of motion and increases conformability to the anatomy for a 38% reduction in tracking forces*1 in challenging anatomies.
As demonstrated in bench testing.
Bench testing may not be indicative of clinical performance.
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.
Resources
Find details on the Evolut™ FX System
Evolut™ TAVI in action
Explore our valve design and the performance of the Evolut™ platform over time.
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*
Performance as compared to Evolut™ PRO+ system as bench testing. Bench testing may not be indicative of clinical performance.
Reference
1
Internal report D00512457 Rev B_PRJ000312 Evolut FX Marketing Claim Test Report. Results obtained with 18Fr (14eFr) System for ventricular movement and tracking force tests.
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.
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