Kuros to Begin Fibrin-PTH Clinical Trial in Spinal Fusion

Kuros Biosciences gained FDA approval for its IND application to initiate a Phase IIA clinical trial evaluating Fibrin-PTH orthobiologic in single-level TLIF to treat degenerative disc disease, with autograft as comparator.

SI-BONE Announces New Positive Coverage for MIS SI Joint Fusion using iFuse

Wellmark Blue Cross Blue Shield established positive coverage for minimally invasive surgical sacroiliac joint fusion using SI-BONE's iFuse Implant System in South Dakota and Iowa.

Nexxt Spine Launches Lordotic TLIF Oblique Interbody

Nexxt Spine launched a Lordotic TLIF Oblique interbody as part of its NEXXT MATRIXX family portfolio.

4WEB Receives FDA Clearance for Cervical Stand Alone System

4WEB received FDA 510(k) clearance for its Cervical Spine Truss System-Stand Alone interbody.

Life Spine Expands International Sales to 30 Countries

Life Spine announced it expanded international sales to 30 countries, including Vietnam and South America.

ApiFix Gains FDA Approval for MID-C Scoliosis Treatment

ApiFix received Humanitarian Device Exemption approval to market the MID-C Minimally Invasive Deformity Correction system to treat adolescent idiopathic scoliosis.