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Medtronic's spine software cleared, Surgalign's partnership and more: 5 device company notes
New data on an augmented reality surgical system and four more updates from spine medtech companies in the last week: -
Surgalign revamps anterior cervical plate system
Surgalign relaunched a new generation of its CervAlign anterior cervical plate for anterior cervical discectomy and fusions. -
Cervical interbody system designed by Dr. Jeffrey Hoskins launches
Nexus Spine launched the Stable-C cervical interbody system for spinal fusions. -
Dr. Pierce Nunley completes 1st commercial cases with Spinal Elements' MIS system
Pierce Nunley, MD, of Specialists Hospital of Shreveport (La.), completed the first two commercial cases with Spinal Elements' Karma MIS system. -
Spine company sees strong 24-month patient outcomes for spinal cord stimulation
Two-year data of Saluda Medical's Evoke spinal cord stimulation system showed strong clinical results. -
Pelvic reconstruction technology gets FDA clearance
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. -
Data supports VisAR effectiveness in spine surgery
Novarad's augmented reality surgical guidance system, VisAR, showed strong results in a new study. -
Surgalign partners to expand access to spine devices
PRIA Healthcare has partnered with Surgalign Holdings to expand access to Surgalign spine devices. -
Medtronic's next-gen predictive spine surgery model cleared
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 fusion alternative device reaches FDA milestone
Empirical Spine had its premarket approval Module II accepted and closed by the FDA for the LimiFlex dynamic sagittal tether. -
6 new trends in orthopedic technology
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. -
Insurer OKs ZimVie's spine device, Accelus lands investment and more: 5 medtech notes
Early study data on 3D-printed implants and four more updates from spine devicemakers since July 6: -
OrthoPediatrics signs agreement with 3D software developer
OrthoPediatrics has signed an agreement with 3D-Side, a Belgian software developer that manufactures patient specific 3D cutting guides. -
3 cervical disc replacement devices get FDA's pre-market approval
Centinel Spine earned FDA approval for three more Prodisc total disc replacement devices. -
Early results show promise for 3D-printed titanium spine implants
Six-month data for Nexxt Spine's Matrixx 3D-printed titanium interbody implant showed strong results compared to poly-ether-ether-ketone devices. -
Minimally invasive implants cleared for lumbar spinal stenosis
Aurora Spine received FDA clearance for its Zip minimally invasive spine implants. -
Implant manufacturer Implanet revenue up 33% in Q2
Medical technology company Implanet has seen its revenue rise in the second quarter. -
Spine devicemaker lands $12M funding
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. -
ZimVie's pediatric scoliosis device gets coverage by Anthem BCBS
Anthem Blue Cross Blue Shield will cover ZimVie's Tether device to treat pediatric scoliosis. -
Former Medtronic employee, contractor charged in $1M fraud, money-laundering scheme
A former employee and contractor of Medtronic's Costa Rica business have been charged with conspiring to defraud the company in a $1 million scheme, according to the U.S. Department of Justice.
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