Julie A. Vetalice, Author at ORTHOWORLD

CoNextions Gains FDA Clearance of Coronet Tenodesis Product

CoNextions was granted FDA 510(k) clearance for the Coronet™ tenodesis system for fixation of tissue to bone and tissue to tissue.

Mar 12, 2020

OSSIO Gains FDA Clearance for OSSIOfiber Hammertoe Fixation

ORTHOFLASH Trauma

OSSIO was granted FDA 510(k) clearance to market the OSSIOfiber® Hammertoe Fixation system.

Mar 12, 2020

DePuy Synthes Announces CE Mark for BI-MENTUM Dual Mobility Hip

Joint Replacement ORTHOFLASH

DePuy Synthes has been informed of CE Mark approval for the BI-MENTUM™ Dual Mobility hip for patients with a higher dislocation risk.

Mar 12, 2020

Arthrosurface OVO with Inlay Glenoid Total Shoulder Study Update

Joint Replacement ORTHOFLASH

Study results indicate that use of Arthrosurface's OVO® with Inlay Glenoid Shoulder Arthroplasty System to treat glenohumeral OA yielded improved clinical outcomes, no reoperations or radiographic loosening and a high rate of return to activity.

Mar 12, 2020

NuVasive Attrax Putty Study Results

Orthobiologics ORTHOFLASH

Study results support the use of NuVasive's Attrax® Putty as a standalone bone graft substitute for autograft in instrumented thoracolumbar posterolateral lumbar fusion.

Mar 10, 2020

OrthoPediatrics Launches Large Fragment Cannulated Screw in U.S.

ORTHOFLASH Trauma

OrthoPediatrics commenced limited U.S. launch of the Large Fragment Cannulated Screw.

Mar 10, 2020

AAOS Cancels 2020 Annual Meeting in Face of COVID-19 Concerns

Competitive Landscape Market Drivers

The 2020 Annual Meeting of the American Academy of Orthopaedic Surgeons (AAOS) is canceled due to the ongoing spread of coronavirus. ORTHOWORLD wishes to reiterate our commitment to keep Members and subscribers apprised of the announcements to follow over the coming weeks.

Mar 10, 2020