Achieves Significant Milestone with Expanded Use Indication, Opens Sizable New SI Market Opportunity ~ LOS GATOS, CA / ACCESS ...

Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain management solutions, today announced that the U.S. Food and ...

Aurora Spine earned FDA 510(k) clearance for its Aero facet fusion system, the devicemaker said March 25. Aero is a minimally ...

Twelve-year-old Aly, the spirited daughter of an Arkansas National Guardsman, is preparing for a crucial surgery to address ...

Spine surgeons performed a rare case on a 9-month-old baby at Indianapolis-based Riley Hospital for Children, Fox 59 reported March 24. The baby girl had congenital vertebral dislocation, a spinal ...

As spine surgery continues to evolve with technological advances and a push toward value-based care, more procedures are ...

Tenon shares are moving higher on Tuesday on possible continued strength after the company announced yesterday that it ...

Cleared for use from spinal levels C2 to S1 (inclusive), the system can be used as a stand-alone facet fusion procedure or as an adjunct to larger spinal fusion surgeries. Engineered for earlier ...

Aurora Spine Corporation ("Aurora Spine" or the "Company") (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain management ...

With this approval, the Catamaran is now indicated to treat the SI joint as either a stand-alone treatment or to augment a spinal fusion. "The FDA has cleared the Catamaran SI Joint Fusion System ...

Cleared for use from spinal levels C2 to S1 (inclusive), the system can be used as a stand-alone facet fusion procedure or as an adjunct to larger spinal fusion surgeries.