The global spine biologics market is set to grow at a compound annual growth rate of 2.07 percent between 2016 and 2020, according to a Reports Web analysis.
San Diego-based NuVasive received FDA clearance for the use of its Reline posterior fixation system to implant the MAGEC system.
William D. Tobler, M.D. and Richard J. Nasca, MD, a pair of respected surgeons, collaborated to write a chapter on the unique paracoccygeal transsacral approach to the lumbosacral junction for interbody fusion in the fourth edition of “Benzel's Spine Surgery:…
The FDA granted 29 orthopedic- and spine-related device clearances in August.
Here are eight key notes on orthopedic and spine device companies over the past week.
Carlsbad, Calif.-based Alphatec made changes to its executive leadership team as well as updated its compliance status with Nasdaq's listing requirements.
The Journal of the American Medical Association published the pivotal trial results for Medtronic's Hybrid Closed Loop system.
Warsaw, Ind.-based Zimmer Biomet acquired Netherlands-based Clinical Graphics.
Atlanta-based Meditech Spine received FDA clearance to market its CURE Anterior Cervical Plate system.
Progenerative Medical entered a technology licensing agreement with Kinetic Concepts, both located in San Antonio.