Interventional Spine Announces FDA Clearance of Lordotic Opticage™

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 disc disease. 

Implanet Receives FDA Clearance and CE Mark for Jazz Claw Implant

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

Medtronic Announces U.S. Launch of Spine Essentials

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