Crosstrees Medical Receives FDA 510(k) Clearance for Pod System

Boulder, Colo.-based Crosstrees Medical received FDA 510(k) clearance for its Percutaneous Vertebral Augmentation Pod System.

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Clearance came after an investigational device exemption study of 135 patients in four countries, including the U.S.

The Pod aims to be an improved vertebral fracture repair device.

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