2288 results found.
                    
Study Validates NuVasive's Porous PEEK Cohere
Study results indicate that NuVasive's porous PEEK technology, used in the Cohere® cervical interbody fusion devi...
Medtronic's Kyphon Cement Cleared for Sacral Fracture
Medtronic gained FDA 510(k) clearance for Kyphon™ HV-R Bone Cement for use in sacroplasty
OrthoPediatrics Announces First RESPONSE Spine Procedure in Japan
OrthoPediatrics marked the first spine surgery in Japan with the RESPONSE™ spine system.
Globus Medical Launches CREO Cement Augmented Pedicle Screw
Globus Medical launched the CREO® Fenestrated Screw, designed for use with FORTRESS™ bone cem...
Safe Orthopaedics Enters Distribution Agreement with KiSCO for Japan
Safe Orthopaedics entered into an exclusive commercialization and distribution agreement in Japan with K...
Kuros Biosciences Begins Trial of MagnetOs in Spinal Fusion
Kuros Biosciences commenced a multicenter study comparing MagnetOs bone graft substitute vs. autologous bone
RTI Surgical Launches Fortilink-TS and -L Interbody Fusion Systems
RTI Surgical launched Fortilink®-TS and -L lumbar interbody fusion systems, which feature
Medacta Marks First US Surgery with MUST SI Joint Screw
Medacta announced the first surgery performed in the U.S. using the Medacta Unconstrained Screw Technology Sacro...
Centinel Spine Gains FDA Clearance of FLX 3D Printed Titanium Interbodies
Centinel Spine received FDA 510(k) clearance to market the FLX™ platform of Integrated Interbody
K2M Launches 100th Product
K2M achieved the milestone of its 100th product following FDA 510(k) clearance and launch of the OZARK™ Cervical Plate
CoreLink Acquiring Expanding Orthopedics
CoreLink has acquired Expanding Orthopedics, developer of the FLXfit™ line of expanding interbody devices. Terms were not disclose...
Implanet Opens UK Sales Branch
Implanet opened a branch in the U.K. to support expansion and growth in the adult degenerative spine market. 
Spineology Rampart One Standard ALIF Interbody Gains Standalone FDA Clearance
Spineology received FDA 510(k) clearance to market the Rampart One™ Standard ALIF device...
Camber Spine Gains FDA Clearance for ENZA-A Titanium ALIF
Camber Spine received FDA 510(k) clearance to market the ENZA™-A Titanium Anterior Lumbar Interbody Fusio...
Safe Orthopaedics Acquires UK Distributor Qspine
Safe Orthopaedics will acquire the salesforce of U.K. distributor Qspine. 
Medicrea Gains FDA Clearance for Patient-Specific Spinal Cage
Medicrea obtained what is reported to be the first FDA 510(k) clearance to market patient-specific spinal cages....
iOrthopedics Reports Patent Awards and Allowances
iOrthopedics has received patent awards and allowances for its Universally Expanding Cage, giving exclusive rights in the
Medtronic Revenue Grows 3.7%
ORTHOWORLD estimates Medtronic’s FY4Q18 revenue at US $787.0MM, +3.7% vs. FY4Q17.
K2M Receives FDA Clearance for BACS Patient-Specific Module
K2M received FDA 510(k) clearance to market BACS® Patient-Specific devices. 
Medacta Launches Customizable MySpine MC Surgical Guides
Medacta announced FDA 510(k) clearance and launch of the MySpine Midline Cortical Pedicle Screw Placement Guide
NuVasive SpineTRACK Registry Reaches 10,000 Enrollment Milestone
NuVasive's SpineTRACK Registry reached a milestone of 10,000 patients enrolled since its inception in 2011. 
Spinal Elements Expands Launch of Clutch Interspinous Process Device
Spinal Elements commenced full launch of the Clutch® interspinous process device for treatment of various poste...
Life Spine Gains FDA Clearance for PRO-LINK Ti Stand-Alone Cervical Spacer
Life Spine received FDA 510(k) clearance to market additional indications for the PRO-LINK®
Zimmer Biomet Gains 510(k) Clearance for Zyston Strut Open Titanium Interbody Spacer
Zimmer Biomet received FDA 510(k) clearance to market the Zyston® Strut Open Titanium Interbody Spac...
Implanet Launches JAZZ Evo® for Adult Degenerative Spine Disease
Implanet launched JAZZ Evo® for adult vertebral fusion. The device is the first in a new range
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