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Future Market Insights (FMI) delivers key insights on the global spinal fusion market in its upcoming report titled “Spinal Fusion Market: Global Industry Analysis 2012–2016 and Opportunity Assessment 2017 – 2027.” In terms of revenue, the global spinal fusion market is projected to register a CAGR of 5.4% over the...
Three separate Texas healthcare providers will pay a collective $1,056,340.50 to resolve liability under the False Claims Act for the alleged improper
® Modular Pedicle Screw System, first introduced by Precision Spine in April 2016, today reaches a monumental milepost, its 30,000 th modular screw implantation. This historic milestone is most impressive when highlighted by the fact that there have been no reported dissociations to date. The Reform ® Modular Pedicle Screw System provides surgeons with increased flexibility, versatility, and visibility to meet the varying requirements of degenerative and trauma procedures. The cobalt chrome and titanium tulips are available in both 5.5 and 4.75mm sizes, with standard and reduction options. ...
Press release content from Business Wire. The AP news staff was not involved in its creation. Precision Spine® Receives FDA 510(K) Clearance for the Dakota ACDF™ Standalone System February 4, 2021 GMT PARSIPPANY, N.J.--(BUSINESS WIRE)--Feb 4, 2021-- Precision Spine, Inc., a medical device company dedicated to Made-in-the-USA manufacturing, announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Dakota ACDF™ Standalone System in the treatment of degenerative disc disease (DDD). The Dakota ACDF system features a titanium plate polyethe...