ST. PAUL, Minn.--(BUSINESS WIRE)--Spineology Inc., an innovator in anatomy-conserving surgery, is excited to announce the FDA grant of its proprietary Spineology Interbody Fusion System, now called ...

Please provide your email address to receive an email when new articles are posted on . Among 61 patients who underwent posterior lumbar interbody fusion, 95.1% achieved fusion. A non-window-type ...

Please provide your email address to receive an email when new articles are posted on . Nvision Biomedical Technologies announced FDA clearance of its 3D-printed PEEK interbody system. The system is ...

Minimally invasive transforaminal lumbar interbody fusion and minimally invasive extraforaminal lumbar interbody fusion are effective techniques for addressing degenerative lumbar spine disorders, and ...

Spine Innovation’s Logic titanium implant system earned FDA 510(k) clearance, according to a Jan. 26 news release. The device ...

Spine Innovation, LLC, a medical device startup that develops novel interbody fusion implants, announced today that is has received FDA 510(k) clearance to market the LOGIC™ Titanium Implant System.

Posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF) procedures are coded 22630 for a lumbar initial interspace arthrodesis, posterior interbody technique, which ...

KNOXVILLE, Tenn.--(BUSINESS WIRE)--ChoiceSpine LLC, a privately held spinal device manufacturer based in Knoxville, TN, successfully announces 3,000 implantations of their innovative 3D Printed Tiger ...

A civil engineer at the University of Pittsburgh is applying his expertise in bridges and infrastructure to develop new materials that better treat spinal injury, repair, and recovery. Amir Alavi’s ...

Interbody cage fusion uses a hollow threaded titanium or carbon fiber cylinder to fuse two vertebrae together. The diseased disc is removed and an interbody cage (s) are placed in the opening where ...