The US Food and Drug Administration (FDA) has granted 510(k) clearance to Amber Implants’ VCFix Spinal System, intended for treating a wide array of vertebral compression fractures. The minimally ...

Medtronic plc has received U.S. FDA 510(k) clearance and breakthrough device designation for its Ligapass 2.0 ligament augmentation system in spine surgery. The surgical treatment is designed to ...

Medtronic’s line of devices to strengthen the spine just got a bit stronger itself. The medtech giant has secured what it says is the FDA’s first clearance for a device to perform ligament ...

Jefferson Health is using new 3D technology for patients who need spinal fusion. This new high-tech back surgery is being used to create personalized spinal implants, and for a Chester County mother, ...

A collaboration between civil engineering and neurosurgery at the University of Pittsburgh could change how spinal fusion surgery is performed and monitored. Associate Professors Amir Alavi, Nitin ...

The Spinal Implants and Surgery Devices Market is witnessing strong growth driven by rising cases of spinal disorders, increasing adoption of minimally invasive procedures, and continuous ...

A tiny, flexible electronic device that wraps around the spinal cord could represent a new approach to the treatment of spinal injuries, which can cause profound disability and paralysis. A team of ...

The surgeon removes the balloon and injects bone cement into the spine. Use CPT 22523 for a thoracic percutaneous vertebral augmentation, including cavity creation (fracture reduction and bone biopsy ...