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

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