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San Ramon, CA, Nov. 19, 2019 -- BioVentrix, Inc., a privately-held company with a first-in-class, transcatheter-based structural heart device to treat heart failure, today announced that the U.S. Food and Drug Administration (FDA) has granted the company Breakthrough Device Designation status for its Revivent TC™ Transcatheter Ventricular Enhancement System for heart failure.


San Ramon, CA, USA – Oct. 07, 2019 – BioVentrix, Inc. announced the first patient was enrolled and treated in the REVIVE-HF European study, a prospective multi-center, dual-arm randomized controlled study evaluating the treatment of ischemic cardiomyopathy induced heart failure with the Revivent TC System compared to Guideline-Directed Medical Therapy (GDMT) or drug treatment. 


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BioVentrix è una società privata di dispositivi medici con sede a San Ramon, in California, negli Stati Uniti.

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© 2020 BioVentrix. Tutti i diritti riservati. Realizzato da MedTech Momentum
Il marchio Revivent TC ™ è un marchio registrato a livello federale di proprietà di BioVentrix. Qualsiasi utilizzo non autorizzato è espressamente vietato.