The FDA has provided 510(k) clearance for Medtronic's UNiD Spine Analyzer v4.0 planning platform, which includes a new Degen Algorithm for degenerative spine procedures.
Spinal Tech
Empirical Spine had its premarket approval Module II accepted and closed by the FDA for the LimiFlex dynamic sagittal tether.
From the growth of telehealth during the COVID-19 pandemic to the ever improving medical technology paving the way, physicians are always looking for new ways to adapt to best serve their patients.
Early study data on 3D-printed implants and four more updates from spine devicemakers since July 6:
OrthoPediatrics has signed an agreement with 3D-Side, a Belgian software developer that manufactures patient specific 3D cutting guides.
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Centinel Spine earned FDA approval for three more Prodisc total disc replacement devices.
Six-month data for Nexxt Spine's Matrixx 3D-printed titanium interbody implant showed strong results compared to poly-ether-ether-ketone devices.
Aurora Spine received FDA clearance for its Zip minimally invasive spine implants.
Medical technology company Implanet has seen its revenue rise in the second quarter.
Privately held medical technology company Accelus has received a $12 million series D investment from Concord Innovation Fund II to accelerate its work on minimally invasive spinal surgery research.