2629 results found.
AmeriHealth Caritas Covers Paradigm Spine’s coflex
AmeriHealth Caritas issued a positive commercial payor policy covering Paradigm Spine
WishBone Medical Acquires Response Ortho
WishBone Medical acquired Response Ortho, a manufacturer of external and internal fixation and deformity correction products for the
Aurora Spine Reports 3Q18 Revenue of $2.7MM, +59.6% vs. 3Q17
Aurora Spine reports 3Q18 revenue of US $2.7MM, +59.6% vs. 3Q17.
Zimmer Biomet Recalls Spinal Fusion and Long Bone Stimulators
Zimmer Biomet initiated a recall of 1,360 units of the Osteogen Implantable Bone Growth Stimulator,...
Safe Orthopaedics Study: Cost Savings with Single-use Instruments
Study results revealed an average 50% cost-per-patient savings with use of Safe Orthopaedics' instruments vs. reusable one...
SurGenTec Launches GraftGun with ViBone Viable Bone Matrix
SurGenTec completed initial clinical launch of the GraftGun bone graft delivery system combined with ViBone
Vertiflex Study: 85% Reduction in Opiod Use after Treatment with Superion
Results from a randomized, controlled trial of Vertiflex's Superion® Indirect Decompression System showed an 85% decrease
Medtronic Reports FY2Q19 Orthopaedic Revenue of $744MM, +0.7% vs. 3Q17
Medtronic reports FY2Q19 orthopaedic revenue of US $744MM, +0.7% vs. 3Q17
Medicrea Reports 3Q18 Revenue of €7.3MM, +14.1% vs. 3Q17
Medicrea reports 3Q18 revenue of €7.3MM (USD $9.0MM), +14.1% vs. 3Q17.
ChoiceSpine Acquired by Altus Capital
ChoiceSpine, a manufacturer of devices and biologics used to treat complex spine disorders, was acquired by Altus Capital Partners.
HealthPartners Covers RTI’s SImmetry SI Joint Fusion
HealthPartners, the largest consumer-governed nonprofit healthcare organization in the U.S., issued a positive coverage decision for minimally invasive sacroiliac joint fusion surgery, expanding patient access to
Aurora Spine Gains Access to SI Fusion Patent
Aurora Spine acquired an exclusive license to a U.S. patent pertinent to sacroiliac joint repair.
NuVasive Launches Brigade for ALIF Surgery
NuVasive announced U.S. commercial launch of the Brigade® Lateral device for lateral anterior lumbar interbody fusio...
Xtant Reports 3Q18 Revenue of $17.3MM, -12.7% vs. 3Q17
Xtant reports 3Q18 revenue of US $17.3MM, -12.7% vs. 3Q17.
Precision OS Gains Funding for Virtual Reality/Pre-op Planning Software
Precision OS Technology secured US $2.3MM in Series A funding in support of its virtual reality orthopaedic surgical educ...
Investors Prioritize Care Delivery, Post-Revenue Companies
By Carolyn LaWell Extremities, sports medicine, digital health and the hospital supply chain remain attractive areas for orthopaedic innovation, according to investors who spoke during the Musculoskeletal New Ventures Conference (MNVC) held in October. This seems like a natural course, ...
Camber Spine: First Procedures with ENZA-A Titanium ALIF
Camber Spine successfully completed its first procedures with the ENZA™-A Titanium Anterior Lumbar Interbody...
Simplify Medical Completes Cervical Disc IDE Trial
Simplify Medical completed enrollment and treatment of all patients in its U.S. Investigational Device Exemption pivotal trial evaluating the Simpl...
Medacta Acquires Balgrist CARD
Medacta invests in personalized medicine by acquiring start-up Balgrist CARD.
Bio2 Gains Approval to Study Vitrium in Interbody Fusion
Bio2 Technologies received FDA approval to enroll subjects in an IDE clinical study of Vitrium bioactive glass as a
Globus Medical Reports 3Q18 Revenue of $169.2MM, +11.5% vs. 3Q17
Globus Medical continues double-digit growth trend, posts 3Q18 revenue of $169.2MM, +11.5%
Alphatec Spine Reports 3Q18 Revenue of $23MM, -0.4% vs. 3Q17
Alphatec Spine reports 3Q18 revenue of US $23MM, -0.4% vs. 3Q17.
K2M Reports 3Q18 Revenue of $71.4MM, +13.9% vs. 3Q17
K2M reports final quarterly results before acquisition by Stryker, posts 3Q18 revenue of $71.4MM, +13.9%
SeaSpine Reports 3Q18 Revenue of $35.8MM, +12.9% vs. 3Q17
SeaSpine picks up momentum, posts 3Q18 revenue of US $35.8MM, +12.9% vs. 3Q17.
NuVasive Gains FDA Clearance for COHERE in XLIF
NuVasive received FDA 510(k) clearance for the COHERE® Porous PEEK™ device in eXtreme Lateral Interbody Fusion
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