The CE Mark is the first regulatory clearance for the system, according to the firm. Mevion also submitted an application for U.S. Food and Drug Administration (FDA) 510(k) clearance in September.
The first Mevion S250i proton therapy system installation in Europe will be completed in 2018. Image courtesy of Mevion Medical Systems.
The firm also announced the first European Mevion S250i proton therapy system installation will be completed in 2018 at the Zuid-Oost Nederland Protonen Therapie Centrum at the Maastro Clinic in Maastricht, the Netherlands.
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