2797 results found.
NuVasive Gains Additional FDA Clearance for CoRoent Small Interlock
NuVasive received FDA 510(k) clearance for expanded indications for the CoRoent Small Interlock™ system.
DePuy Synthes Launches SYMPHONY OCT System
DePuy Synthes launched the SYMPHONY Occipito-Cervico-Thoracic System, expanding its offering for the treatment of conditions in the neck and upper spine.
SpineOvations Launches Clinical Study of DiscSeal for Disc Augmentation
SpineOvations began a clinical study of DiscSeal percutaneous injection for the treatment of low back pain.
4WEB Medical Launches Stand Alone Cervical Spine Truss
4WEB Medical commenced limited launch of the Cervical Spine Truss System-Stand Alone™ (CSTS-SA) implant.
Medtronic’s Surgical Synergy Strategy Accelerates Growth in Spine
Medtronic reports FY 2Q20 orthopedic revenue of USD $828.7 million, +7.2% vs. FY 2Q19.
Life Spine's CENTERLINE Modular Spinal System in Limited Launch
Life Spine commenced limited launch of the CENTERLINE® Modular Thoracolumbar Spinal System, and announced initial surgeries. Full launch is slated for early...
Medicrea Growth Driven by U.S. Sales of Patient-Specific Implants
Medicrea reports 3Q19 revenue of €8.2MM (USD $9.2MM), +12.3% vs. 3Q18.
SI-BONE Continues Growth with Reimbursement Wins
SI-BONE reports 3Q19 revenue of USD $16.2MM, +20.9% vs. 3Q18.
OrthoPediatrics Records Highest Revenue Quarter in Company History
OrthoPediatrics reports 3Q19 revenue of USD $20.7MM, +31.1% vs. 3Q18.
Xtant Taps New CEO to Lead Turnaround Effort
Xtant reports 3Q19 revenue of USD $15.7MM, -8.9% vs. 3Q18.
Globus Medical Double-Digit Growth Driven by Spinal Hardware and ExcelsiusGPS
Globus Medical reports 3Q19 revenue of USD $196.2MM, +15.9% vs. 3Q18.
Zimmer Biomet Gains Momentum on ROSA Knee and Increased Supply
Zimmer Biomet reports 3Q19 orthopedic revenue of USD $1,686.8MM, +3% vs. 3Q18.
RTI Surgical Reduces Guidance Due to Softer than Expected coflex Sales
RTI Surgical reports 3Q19 orthopedic revenue of USD $65.7MM, +10.7% vs. 3Q18.
CMS Increases Medicare Physician Payment for Minimally Invasive SI Joint Fusion
CMS increased the Medicare Physician Fee Schedule for CPT® Code 27279, Arthrodesis Sacroiliac Joint, under which minimally invasive sacroiliac j...
DiFusion Gains FDA Clearance for Xiphos ZFUZE Biomaterial
DiFusion received FDA 510(k) clearance for the Xiphos-ZF spinal interbody device made from ZFUZE biomaterial. Product launch will occur within 4Q19.
U.S. Spinal Hardware Sales Continues to Drive NuVasive Growth
NuVasive reports 3Q19 revenue of USD $290.8MM, +7.2% vs. 3Q18.
Alphatec Spine Continues Success Story with New Product Launches and a Revitalized Sales Channel
Alphatec Spine reports 3Q19 revenue of USD $29.2MM, +26.9% vs. 3Q18.
Stryker Gains FDA Clearance for SAHARA Lateral 3D Expandable Interbody
Stryker received FDA 510(k) clearance to market the SAHARA® Lateral 3D Expandable Interbody System featuring Lamellar 3D Titanium Technology.
Spinal Implant Growth Drives SeaSpine to Record Revenues
SeaSpine reports 3Q19 revenue of USD $39.9MM, +11.3% vs. 3Q18.
Orthofix Weighed Down by Management Vacancies and Order Delays
Orthofix reports 3Q19 revenue of USD $113.5MM, +1.6% vs. 3Q18.
DePuy Synthes to Promote TINAVI Robotic Solutions in China
DePuy Synthes will promote TINAVI’s robotic applications for spine and trauma surgery in China.
Settlement of FCA Allegations Against Life Spine
Life Spine and certain of its executives agreed to pay $6MM to resolve a civil healthcare fraud lawsuit alleging violations of the False Claims Act. 
Safe Orthopaedics SteriSpine LC and CC Gain Japan Regulatory Approval
Safe Orthopaedics received regulatory approval for SteriSpine™ LC lumbar and CC cervical cages in Japan.
3 Questions on the Spine Reimbursement Environment
By Carolyn LaWell, ORTHOWORLD The spine market’s evolving reimbursement landscape can be hard for device companies and surgeons to navigate. While at NASS, we asked reimbursement expert Kim Norton for a high-level view of the reimbursement shifts taking place today. Ms. Norton is ...
Nanovis Gains FDA Clearance for Bioceramic Nanotube Surface
Nanovis received the first FDA 510(k) clearance for a bioceramic nanotube surface that demonstrates FDA's requirements for nanotechnology.
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