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The EDWARDS INTUITY valve system demonstrated a significantly larger effective orifice area (EOA) at 1 year compared with conventional bioprosthesis for FS1
MIAVR with EDWARDS INTUITY valve system demonstrated stable mean and peak gradients over time compared to conventional bioprosthesis for FS1
For more information, please click on the icon below to download the CADENCE-MIS trial summary.
References
AVR, Aortic Valve Replacement; FS, Full Sternotomy; MIS, Minimally Invasive Surgery; MIAVR, Minimally Invasive Aortic Valve Replacement; RDAVR, Rapid Deployment* Aortic Valve Replacement
* Simplified implantation through reduced suture steps
**Results based on the first generation of the EDWARDS INTUITY valve system, Model 8300A
For professional use. See instructions for use for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.
Edwards Lifesciences devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.
Edwards, Edwards Lifesciences, the stylized E logo, CADENCE, CADENCE-MIS, Carpentier-Edwards, EDWARDS INTUITY, EDWARDS INTUITY Elite, PERIMOUNT and ThermaFix are trademarks of Edwards Lifesciences Corporation or its affiliates. All the other trademarks are the property of their respective owners.
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