30 Day Trial

Medtronic's Kyphon Cement Cleared for Sacral Fracture

Medtronic gained FDA 510(k) clearance for Kyphon™ HV-R Bone Cement for use in sacroplasty.

Study Validates NuVasive's Porous PEEK Cohere

Study results indicate that NuVasive's porous PEEK technology, used in the Cohere® cervical interbody fusion device, presents a clinically viable option to improve osseointegration and fusion.

Anika Therapeutics Announces Top-Line Results from CINGAL Trial in Knee OA

In the Phase III 16-02 clinical trial of Anika Therapeutics' CINGAL, statistically significant results in pain reduction were not demonstrated at the primary endpoint of 26 weeks.

DePuy Synthes Launches DYNACORD Suture

DePuy Synthes Mitek Sports Medicine commenced limited U.S. launch of DYNACORD Suture. Full launch is slated for 3Q18.

Arthrosurface Trial Results with PF Wave Implant

Five-year midterm clinical study results reconfirmed joint preservation in patellofemoral surgery using Arthrosurface's PF Wave™ implant.

OrthoPediatrics Announces First RESPONSE Spine Procedure in Japan

OrthoPediatrics marked the first spine surgery in Japan with the RESPONSE™ spine system.

Medacta Gains FDA Clearance for Short Humeral Diaphysis

Medacta received FDA 510(k) clearance for a Short Humeral Diaphysis used with the Medacta Shoulder System. 

OrthoGrid Launches HipGrid NINE for Outpatient Total Hip Replacement

OrthoGrid Systems launched the HipGrid® NINE radiographic assessment and alignment system for outpatient total hip replacement. 

Globus Medical Launches CREO Cement Augmented Pedicle Screw

Globus Medical launched the CREO® Fenestrated Screw, designed for use with FORTRESS™ bone cement to treat thoracolumbar spinal tumors.

Wright Medical Gains FDA Premarket Approval for AUGMENT Injectable Bone Graft

Wright Medical received FDA premarket approval for AUGMENT® Injectable Bone Graft, serving as an alternative to autograft in hindfoot and ankle fusion.


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