The U.S. Food and Drug Administration issued a Class 1 recall for Stryker Spine's OASYS Midline Occiput Plate.
Spinal Tech
A New Jersey court has determined two Biomet subsidiaries still owe $2.7 million in royalty payments to spine surgeon Neil Kahanovitz, MD, after they stopped paying him in 2008, according to a Mass Device report.
Carlsbad, Calif.-based Aurora Spine's new expanded corporate headquarters has opened.
San Francisco-based SpineGuard received FDA 510(k) clearance for three products to complete its PediGuard platform of single-use drilling instruments for pedicle screw pilot holes.
LDR's Mobi-C cervical disc replacement recently received FDA market approval for two-level indications and became the first device to be endorsed for multiple level indications in the cervical spine.
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Austin, Texas-based LDR Holding has filed a proposed initial public offering form with the Securities and Exchange Commission for its common stock.
Austin, Texas-based LDR's Mobi-C Cervical Disc has been approved by the FDA for two-level indications, making it the only cervical disc in the country approved to treat more than one level in the cervical spine.
NuVasive, based in San Diego, has relocated its United Kingdom office to an expanded location. The new facility is a two-story, 7,500-square-foot building in London.
Irvine, Calif.-based Interventional Spine received a patent related to the Opticage expandable fusion cage and PerX360 system for minimally invasive lumbar interbody fusion.
East Providence, R.I.-based IlluminOss Medical appointed Dwayne Montgomery, MBA, as senior vice president of sales and marketing.