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Dritte FDA-Zulassung für revolutionäres Simbionix-Produkt
Date:3/31/2013

CLEVELAND, March 31, 2013 /PRNewswire/ --

Die Simbionix USA Corporation, einer der weltweit führenden Anbieter für medizinische Ausbildung und Simulationstraining, hat die FDA-Zulassung für die Anwendung TEVAR (thorakale endovaskuläre Aneurysmabehandlung) für PROcedure Rehearsal Studio™ (PRS) erhalten. Die Anwendung ist eine weitere Komponente der PRS-Familie, die zur Vermarktung für Eingriffe an der Halsschlagader und EVAR-Eingriffe (endovaskuläre Aneurysmabehandlung) zugelassen wurde.

     (Logo: http://photos.prnewswire.com/prnh/20120502/529202-a)

TEVAR ist eine neue Behandlungsmethode, die von Medizinern für die Behandlung von thorakalen Aortaerkrankungen schnell angenommen wurde. Der Eingriff ist weitaus weniger invasiv als eine offene Operation. Zudem hat die Verfügbarkeit und relativ leichte Anwendung von TEVAR die Behandlungsoptionen für thorakale Aortaerkrankungen verändert und erweitert, unter anderem bei Patienten, bei denen eine offene Operation nicht in Frage kommt. Für die Anwendung von TEVAR ist eine spezielle fachliche Schulung erforderlich, da sie erhebliche perzeptive, kognitive und psychomotorische Leistungen seitens der Chirurgen erfordert.

Das PROcedure Rehearsal Studio verwendet eine revolutionäre, von Simbionix entwickelte Technologie, mit der Mediziner in der Lage sind, einen kompletten endovaskulären Eingriff an einem virtuellen anatomischen 3D-Modell auf Basis spezifischer CT-Daten eines Patienten zu übe
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SOURCE Simbionix USA Corporation
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