Der Eingriff fand Ende Juli im Harborview Medical Center in Seattle, USA, im Rahmen einer von der FDA erteilten Investigational Device Exemption (IDE) statt. Unter der Leitung von Dr. Jeffrey G. Ojemann, MD, von der University of Washington School of Medicine in Seattle und dem Co-Studienleiter Professor Steven C. Cramer von der University of California, Los Angeles, werden in dieser Studie erste Sicherheitsdaten erhoben
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