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....
Jun 14, 2018,
Spine
ORTHOFLASHRTI Surgical Launches Fortilink-TS and -L Interbody Fusion Systems
RTI Surgical launched Fortilink®-TS and -L lumbar interbody fusion systems, which feature TETRAfuse® 3D printed polymer....
Jun 12, 2018, Julie Vetalice
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-Iliac Joint Screw (M.U.S.T. SI) for sacroiliac...
Jun 11, 2018, Julie Vetalice
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 and non-integrated interbody fusion devices....
Jun 08, 2018, Julie Vetalice
K2M Launches 100th Product
K2M achieved the milestone of its 100th product following FDA 510(k) clearance and launch of the OZARK Cervical Plate....
Jun 07, 2018, Julie Vetalice
Spineology Rampart One Standard ALIF Interbody Gains Standalone FDA Clearance
Spineology received FDA 510(k) clearance to market the Rampart One Standard ALIF device without supplemental fixation....
Jun 05, 2018, Julie Vetalice
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 Fusion system....
Jun 04, 2018, Julie Vetalice
iOrthopedics Reports Patent Awards and Allowances
iOrthopedics has received patent awards and allowances for its Universally Expanding Cage, giving exclusive rights in the expandable interbody arena....
Jun 01, 2018, Julie Vetalice
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....
Jun 01, 2018, Julie Vetalice
K2M Receives FDA Clearance for BACS Patient-Specific Module
K2M received FDA 510(k) clearance to market BACS® Patient-Specific devices. ...
May 30, 2018, Julie Vetalice
Loading new posts...
No more posts
