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NuVasive sued by analytics company; contract breach alleged
Trilliant Health is suing NuVasive for $1 million over allegations that the spine devicemaker breached a five-year agreement. -
Neurosurgeon joins Medtronic as chief medical officer of neuromodulation
Medtronic hired Ashwini Sharan, MD, as chief medical officer of the company's neuromodulation operating unit. -
Metal-based interbody spine implants to see highest growth by 2030
Metal-based implants are expected to be the fastest-growing segment in the interbody spine implant market, according to research from business consulting firm Prescient & Strategic Intelligence. -
Current and future uses of Kambin's triangle in spine surgery
Kambin's triangle, an access point in the spine, is commonly used to perform lumbar interbody fusions. A review of current and future uses of Kambin's triangle was published June 6 in Cureus. -
Color-coded interbody device approved by FDA
Aurora Spine received FDA clearance for its Dexa Solo-LTM anterior lumbar fusion device on the heels of record first-quarter sales. -
3D spine surgery planning system gets FDA clearance
SMAIO got FDA clearance for the Balance Analyzer 3D planning software for spine realignment. -
Devicemaker adds senior vice president of product development
Intelligent Implants added Andy Forsberg as senior vice president of product development. -
CTL Amedica executive recognized as top spine inventor
CTL Amedica Chief Technology Office Sean Suh was included on Spinemarket's top spine inventor list for the sixth year in a row. -
Spinal implant system more cost-effective than TLIF, study finds
Premia Spine's Tops spinal arthroplasty system was found to be more cost-effective than a transforaminal lumbar interbody fusion, according to a study published in the Journal of Health Economics and Outcomes Research. -
Medtronic's quarterly earnings, Stryker's FDA approval and more: 6 device company notes
Two companies see record quarterly sales and five more updates from spine devicemakers in the last week: -
SI-Bone's pelvic fixation device gets FDA nod
SI-Bone's iFuse Bedrock Granite implant system for sacroiliac fusion and sacropelvic fixation received FDA clearance. -
Stryker spinal imaging system gets FDA clearance
Stryker's Q guidance system received FDA 510(k) clearance for spine surgery applications. -
2 spine devicemakers see record Q1 revenue
Two spine medtech companies saw their best first-quarter sales in 2022. -
Spine device company opens robotic research, surgical training labs
Medical technology company Accelus opened its new robotic research and development lab in Louisville, Colo., and clinical education and surgical training lab in Carlsbad, Calif., bringing it one step closer to its goal of making minimally invasive surgery the industry standard for spine care. -
Zimmer Biomet names communications, administration exec
Zimmer Biomet named Keri Mattox as chief communications and administrator officer. -
Medtronic Q4 spine sales fall, full-year sales grow: 5 notes
Medtronic on May 26 posted a dip in spine sales in the fourth quarter of fiscal year 2022. -
Aurora Spine's record Q1, a new spine table debuts and more: 6 device company notes
Spinal Simplicity's latest hire and five more updates from spine device companies in the last week: -
Texas spine center enrolls 10th patient in multilevel disc replacement trial
Texas Spine Care Center in San Antonio has enrolled its 10th patient in a trial comparing the safety and effectiveness of Centinel Spine's disc replacement products to a similar FDA-approved product. -
Idaho hospital debuts spine surgery operating table
Northwest Specialty Hospital in Post Falls, Idaho, added the ProAxis spinal surgery table. -
7 recent device company leadership moves
From CEO shifts to board of directors reshuffling, here are seven device company leadership appointments covered by Becker's since April 26:
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