Crosstrees Medical Receives FDA 510(k) Clearance for Next Generation Device for Percutaneous Vertebral Augmentation

Crosstrees Medical announced that it has received 510(k) clearance from the FDA for the Crosstrees PVA Pod System for Percutaneous Vertebral Augmentation. FDA clearance was based on a prospective, single-arm IDE study that enrolled 135 patients in the U.S., China, Venezuela and Belgium.
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