Spine

Intellirod Spine gained FDA de novo clearance for the LOADPRO® disposable spinal rod strain sensor, initially for use with Xtant Medical's FORTEX...

NuVasive announced initial XLIF® spinal procedures using the Cohere® XLIF lateral Porous PEEK device....

SpineEX was issued its second U.S. patent, addressing a novel mechanism to adjust posterior and anterior sides of an interbody...

Alphatec announced commercial release of the IdentiTi-C Porous Titanium Interbody for ACDF....

MiRus received FDA 510(k) clearance for the Europa pedicle screw made of MoRe® molybdenum rhenium superalloy material....

SpineEX gained additional FDA clearance for the Sagittae Lateral Lumbar Interbody Fusion system, covering new instrumentation and an updated surgical technique....

RTI Surgical enrolled the first patient in FORTE, a clinical evaluation of the Fortilink® interbody fusion device in the treatment of...

Implanet received FDA 510(k) clearance to market JAZZ Cap® to secure screws in poor quality bone in vertebral fusion procedures....

AxioMed was issued approval under the CE Mark for their viscoelastic cervical disc replacement....

The use of 3D-Side's bone-cutting jigs in the treatment of bone tumors is now fully reimbursed by local regulatory authorities in France,...