30 Day Trial

Spineway Mont Blanc MIS Approved in Japan

Spineway obtained regulatory approval in Japan for its Mont Blanc minimally invasive surgical devices.

Episurf Medical Granted Patent Approval in the U.K.

Episurf Medical was issued an Intention to Grant for a patent addressing damage marking technology for use in knee repair.

Zimmer Biomet Launches TrellOss-TC Porous Titanium Interbody System

Zimmer Biomet launched the TrellOss™-TC Porous Titanium Interbody, completing its initial offering of porous titanium implants.

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.

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 and function in all patient reported outcomes.

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 pain relief and increased range of motion in patients with glenohumeral arthritis.

Aegis Spine Gains FDA Clearance for AccelFix Expandable Cage

Aegis Spine received FDA 510(k) clearance to market the AccelFix Expandable Cage System.

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.

HD LifeSciences Announces Fluid Channels Patent Allowance

HD LifeSciences received a patent allowance notice addressing fluid channel technology employed in its interbody fusion devices. 

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. 

 



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