CareFusion, a San Diego-based medical technology corporation, received FDA 510(k) clearance for two of its spine augmentation devices.
Spinal Tech
The German Fiagon AG and the German joimax announced their partnership today during the DWG German Spine Congress in Frankfurt, Germany.
NuVasive has selected a site in West Carrollton, Ohio as the location for the build-out of its new medical device facility.
Here are five recent mergers and acquisitions that took place among spine and orthopedic companies.
In a recent press release, DJO Global, Inc. announcedplans to exit Empi business and focus on higher growth Bracing, Surgical and International segments.
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The North American spine surgery devices market is expected to grow to 2019, based on a report from MicromarketMonitor, according to WhaTech.
Medtronic received FDA clearance for the Activa portfolio of Deep Brain Stimulation neurostimulators under the full-body MRI.
Greatbatch has received FDA pre-market approval for its Algovita spinal cord stimulation system, according to a Mass Device report.
PolyPid enrolled the first patient in its clinical trial of BonyPid-1000.
An FDA advisory panel will meet to consider Medtronic's pre-market approval application for its DIAM spinal stabilization system, according to a Mass Device report.