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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Overview
Explore the Evolut™ FX+ system.
Built on the original CoreValveTM 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.
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.
Education and resources
Find more details TAVI information, educational resources, and tools.
Evolut™ 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.
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