Two-year data of Saluda Medical's Evoke spinal cord stimulation system showed strong clinical results.
Spinal Tech
Onkos Surgical has received 510(k) FDA clearance for its My3D pelvic reconstruction system, which includes 3D implants, instruments and models that can be used to treat pelvic issues more effectively, the 3D Printing Media Network reported July 17.
Novarad's augmented reality surgical guidance system, VisAR, showed strong results in a new study.
PRIA Healthcare has partnered with Surgalign Holdings to expand access to Surgalign spine devices.
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.
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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.
Centinel Spine earned FDA approval for three more Prodisc total disc replacement devices.