Gore lands CE Mark for Viabahn vascular device

Gore Medical receives CE Mark approval in the European Union for its Viabahn vascular device for the treatment of obstructed peripheral veins in hemodialysis patients.

Gore Medical said it received CE Mark approval for its Viabahn vascular device for the treatment of obstructed peripheral veins in hemodialysis patients.

The Flagstaff, Ariz.-based company said the approval covers the treatment of obstructed peripheral veins, excluding the venae cavae and pulmonary veins.

W.L. Gore & Associates, Food & Drug Administration (FDA)

News Well, Peripheral Artery Disease, Pre-Market Approval (PMA)

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