Vertos Medical Enrolls in New MOTION Study of MILD Procedure

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

FDA Approves Update of Mobi-C Cervical Disc Labeling to Include 7-Year Clinical Results

FDA approved an update to the labeling for Zimmer Biomet's Mobi-C® Cervical Disc to include 7-year clinical results, showing the device to be statistically non-inferior in overall study success for 1-level use and statistically superior in overall study success for 2-level use.

Alphatec Gains FDA Clearance for OsseoScrew

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

Renovis Surgical Receives FDA Clearance for Tesera X Lateral Interbody Fusion System

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