Spine

SI-BONE's iFuse Implant System®, introduced in 2009, has been used in >40,000 SI joint fusion procedures by more than 1,900 surgeons...

Innovasis was granted FDA 510(k) clearance to market the LxHA Lateral Interbody Fusion Device....

Life Spine received FDA 510(k) clearance to market the PROLIFT® Lateral Expandable Spacer system....

Medicrea was allowed three new U.S. patents relating to the company's proprietary UNiD® Adaptive Spine Intelligence software platform....

NuVasive commenced launch of Modulus® TLIF-O, a porous titanium implant for transforaminal lumbar interbody fusion....

ulrich medical USA is slated to achieve the milestone of 100,000 total vertebral body replacement device implantations within the year....

Aidoc was granted FDA 510(k) clearance to market an artificial intelligence solution to triage cervical spine fractures....

Implanet's JAZZ® Cap device has been successfully used in first U.S. spinal fusion procedures....

RTI Surgical achieved the milestone of 5,000 implants of Fortilink®-C, -TS and -L interbody fusion systems in the U.S....

Zavation received FDA 510(k) clearance to market the Ti3Z lumbar interbody system....