VUZE Medical has received 510(k) clearance from the US Food and Drug Administration (FDA) for its second-generation VUZE system, as per a recent press release from the company
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A recent @SpinalNewsInt guest article saw Arthur L Jenkins III outline what he perceives as the current and future landscape of #Spinal surgery—outlining existing and novel technologies, as well as the potential impact of malpractice premiums in the USA
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.@CentinelSpine recently announced the completion of the 5,000th case in the USA with its prodisc C Vivo and prodisc C SK cervical total disc replacement (TDR) technologies, which are part of the company's new Match-the-Disc system
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.@Woven_Ortho announced recently that it has received its second 510(k) clearance from the US Food and Drug Administration for the use of the Ogmend implant enhancement system in spine surgery
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Spineart has announced that it has successfully raised CHF20 million in convertible financing—an announcement that follows the completion of enrolment in the company’s two BAGUERA C investigational device exemption (IDE) studies
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.@onwdempowered announced recently that it has been awarded Breakthrough Device designation (BDD) by the US Food and Drug Administration (FDA) for the ARC-BCI system
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.@theradaptive recently gained approval from the US Food and Drug Administration (FDA) for its investigational device exemption (IDE) submission to begin enrolling patients into OASIS—a global Phase I/II feasibility study in spine fusion
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Researchers in Italy have demonstrated that an innovative nanovector (nanogel)—which they developed—is able to deliver anti-inflammatory drugs in a targeted manner into glial cells actively involved in the evolution of #Spinal cord injury
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Researchers at @MUSChealth have retrospectively compared the operative microscope to the 3D exoscope in a study of spine surgery procedures, now published in @WorldNeurosurg, and found potentially better outcomes for surgeons/patients alike with the latter
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3Spine has announced the achievement of completed US clinical trial enrolment, with 151 completed MOTUS lumbar total joint replacement surgeries and 174 real-world posterior lumbar fusions—as of December 2023
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SynerFuse has announced the appointment of Rohan Lall (M Health Fairview Neurosurgery, Princeton, USA) as the company’s chief medical officer, effective since 2 January 2024
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Cerapedics has today announced that it has filed the final module in a premarket approval (PMA) application with the US Food and Drug Administration (FDA) for its investigational P-15 peptide enhanced bone graft
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.@mirusmed has announced that it has gained @US_FDA 510(k) clearance for its CYGNUS MoRe anterior cervical plate and Mirus 3DR lateral lumbar interbody fusion system with integrated MoRe plate fixation
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.@CerapedicsInc has announced long-term follow-up data from its pivotal IDE study of the i-FACTOR peptide-enhanced bone graft, demonstrating fusion rates in single-level ACDF of 98.6% after six years
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