14545 results found.
THINK Surgical Gains FDA Clearance for Robotic Knee Replacement Application
THINK Surgical received FDA 510(k) clearance to market the TSolution One® Total Knee Application for pre-surgical planning.
HD LifeSciences Announces Fluid Channels Patent Allowance
HD LifeSciences received a patent allowance notice addressing fluid channel technology employed in its interbody fusion devices. 
Medacta Gains CE Mark for Lateralized Glenosphere
Medacta received CE Mark approval for a lateralized glenosphere component, expanding its range of reverse shoulder replacement options.
Aegis Spine Gains FDA Clearance for AccelFix Expandable Cage
Aegis Spine received FDA 510(k) clearance to market the AccelFix Expandable Cage System.
Arthrosurface OVO with Inlay Glenoid Total Shoulder Study Update
Results of a study of Arthrosurface's OVO® with Inlay Glenoid Shoulder Arthroplasty System demonstrated excellent clinical benefits, including pai...
Smith & Nephew NOVOSTITCH Meniscal Repair Study Update
One-year results from a study of Smith & Nephew's NOVOSTITCH Meniscal Repair demonstrated a success rate of 91.7% and significant improvement in knee pain a...
Spineology Raises $7MM in Equity
Spineology raised $7MM of a potential $16MM round of equity funding.
U.K.'s NICE Maintains Recommendation for Bioventus' EXOGEN
The National Institute for Health and Clinical Excellence in the U.K. updated its guidance regarding use of Bioventus' EXOGEN® Ultrasound Bone Healing S...
Viseon's First Clinical Use of Voyant Lateral System
Viseon announced the first clinical use of Voyant Lateral visualization to support real-time imaging during a minimally invasive lateral lumbar procedure.
Amplify Surgical Announces 100th Level Treated with dualX Expanding Interbody
Amplify Surgical marked the milestone of 100 surgical levels implanted with the dualX™ Expanding Interbody Fusion System.
ADAM Project to Launch Clinical Trials of 3D-Printed Synthetic Bone
ADAM, a 3D bone printing project, plans to complete pre-clinical trials within the month and commence first human trials by the end of 2019.  ...
Paragon 28 Introduces PRECISION Reduction Guide
Paragon 28 launched the PRECISION® Reduction Guide for its Joust™ Beaming Screw System.
Exactech Launches Fixed Bearing Flat Cut Talus Ankle Implant
Exactech expanded the Vantage® Total Ankle Fixed Bearing System with launch of the Vantage Ankle Flat Cut Talus option.
Nextremity Solutions Launches Stratum MPJ Plates
Nextremity Solutions commenced full commercial launch of the Stratum™ MPJ Plating System.
NASS Review: Spinal Robotics, Enabling Technologies, 3D Printing and Biologics
By Mike Evers Enabling technology was the story of the North American Spine Society 2019 annual meeting (NASS), with the top spine players heavily featuring their robotic-assisted surgery ecosystems. These players are becoming clearer in their messaging about how their technologies inte...
Epica Gains FDA Clearance for SeeFactorCT3
Epica was granted FDA 510(k) clearance to market the SeeFactorCT3™ Imaging Platform, comprising computed tomography, fluoroscopy and digital radiography in one syst...
Centinel Spine Marks 18 Years of prodisc L Use in the U.S.
Centinel Spine announced the milestone of the 18th year of clinical usage of prodisc® L in the U.S.
Sectra Adds DePuy Synthes 3D Trauma Templates to Surgical Planning Solution
Sectra added DePuy Synthes' 3D templates to its pre-operative planning tool for trauma procedures.
Turner Imaging Gains FDA Clearance for Smart-C Mini-C Arm
Turner Imaging Systems received FDA 510(k) clearance to market the Smart-C Mini-C Arm Portable Fluoroscopy and X-Ray Imaging Device.
Personalized Stem Cells Enrolls in Clinical Trial for Treatment of OA with Stem Cells
Personalized Stem Cells enrolled the first patients in an FDA-approved clinical trial for treatment of knee osteoarthritis with stem cells.
Pixee Medical Gains Funding for Augmented Reality Tools
Pixee Medical closed a €2MM Series A funding to support global commercialization of augmented reality tools for surgical planning and navigation. ...
Back 2 Basics Gains FDA Clearance for Carbon Interbody Cages
Back 2 Basics received FDA 510(k) clearance to market eCarbon anterior cervical and posterior lumbar Interbody devices.
Conformis and Stryker Enter Development, License and Distribution Agreement for PSI Knee Technology
Conformis and Stryker entered development, license and distribution agreements for patient specific instrument technology. 
Zimmer Biomet Recalls Certain Legacy Biomet Products
Zimmer Biomet voluntarily recalled various legacy Biomet products due to cleaning processes that could lead to elevated bacterial endotoxin and residual debris...
curasan Gains CE Mark for Spinevisc Hyaluronic Acid
curasan is launching Spinevisc® hyaluronic acid for the treatment of facet syndrome.
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