Spine

SI-BONE received an additional FDA 510(k) clearance for use of iFuse Bedrock technology in fusion of the sacroiliac joint during long...

NuVasive is introducing the X360 system integrated with Pulse automation for lateral single-position surgery. ...

Full 2-year outcomes from a U.S. IDE study of Orthofix Medical's M6-C artificial cervical disc demonstrated that disc replacement with...

SpineFrontier was issued a U.S. patent protecting a method for posterior cervical decompression using the LESplasty laminoplasty device....

ChoiceSpine received expanded FDA 510(k) clearance for the HAWKEYE Ti vertebral body replacement for use in the cervical 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....