Spineology received FDA 510(k) clearance to market the Rampart™ Duo™ Interbody Fusion System, reportedly the first device to combine PEEK, titanium and graft containment mesh elements.
The North American Spine Society/NASS issued first of its kind coverage recommendations for electrical bone growth stimulators as an adjunct to spinal fusion, supporting use of pulsed electromagnetic field stim devices, such as Orthofix’s CervicalStim™ and SpinalStimâ„¢.Â
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