Spine

SpineEX received FDA 510(k) clearance to market its Sagittae® expandable device for minimally invasive lateral lumbar interbody fusion. ...

The ApiFix Minimally Invasive Deformity Correction (MID-C) technology for correction of Adolescent Idiopathic Scoliosis has been used in 250 patients...

The U.K.'s National Institute for Health and Care Excellence published medical technology guidance recommending SI-BONE's iFuse® for the treatment of chronic sacroiliac joint pain....

Vertos Medical enrolled the first patient into MOTION, a new multicenter two-year U.S. study of the mild® outpatient procedure for...

FDA approved an update to the labeling for Zimmer Biomet's Mobi-C® Cervical Disc to include 7-year clinical results, showing the...

Renovis Surgical received FDA 510(k) clearance to market the Tesera® X Lateral Interbody Fusion system....

Alphatec received FDA 510(k) clearance to market the OsseoScrew® expandable pedicle screw. ...

DePuy Synthes introduced SENTIO MMG, a digital system to assess nerve status and identify and avoid peripheral nerves during spine surgery....

Stryker received FDA 510(k) clearance for the SpineJack® implantable reduction system to treat osteoporotic vertebral compression fractures....

NuVasive commenced patient enrollment in a prospective, multicenter U.S. study evaluating advanced spinal implants used in XLIF® procedures....