The FDA granted 510(k) clearance to Ascendx Spine for its VCF Repair System for vertebral compression fractures. The VCF system allows physicians to place a single bolus of bone cement in a vertebra with the balloon inflated.
This product, along with the Ascendx Acu-Cut Vertebral Augmentation System, is approved for marketing in Europe.
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This product, along with the Ascendx Acu-Cut Vertebral Augmentation System, is approved for marketing in Europe.
More Articles on Devices:
NuVasive Fusion Cages Receive Japanese Approval
12 Orthopedic Device Company Leadership Moves
Orthofix Pays $43M in Bone Growth Stimulation Settlement