Spine

Tyber Medical’s interbody spinal device line has been accepted into the Australian Registry of Therapeutic Goods. Private label partners are slated...

Ortho Kinematics received Health Canada approval for its lead product, Vertebral Motion Analysis, a diagnostic test for the assessment of spinal motion...

Centinel Spine expanded its MIDLINE II-Ti product family, a Ti-ACTIVE™ coated, No-Profile, anterior lumbar Integrated Interbody device, in the U.S. and Australia....

Vertebral Technologies launched the InterLink™ pedicle screw system, including 22 polyaxial pedicle screws, 19 spinal rods, cross-connectors and set screws, to be used for single...

Interventional Spine announced FDA clearance of the 80 Lumbar Lordotic Opticage™, an intervertebral body fusion device for use with autogenous bone graft in patients with degenerative...

Implanet received FDA 510(k) clearance and CE Mark approval for the Jazz Claw®, a hybrid implant designed to treat degenerative spinal pathologies....

Medtronic commenced U.S. launch of Spine Essentials™, implants and instruments designed to lend efficiency to the most common cervical fusion procedures....

Orthofix announced FDA 510(k) clearance and U.S. limited launch of the FORZA® PTC™ (Peek Titanium Composite) Spacer....

Xtant Medical received FDA 510(k) clearance of a posterior cervical screw indication for the Certex® Spinal Fixation system....

Life Spine announced successful completion of initial cases with the PROLIFT® Expandable Interbody System for minimally invasive PLIF, TLIF and...