CTL Gains FDA Approval for Seurat Pedicle Screw
CTL Medical gained FDA 510(k) clearance to market the SEURAT Universal Pedicle Screw. The product is slated for 2H18 launch....
CTL Medical gained FDA 510(k) clearance to market the SEURAT Universal Pedicle Screw. The product is slated for 2H18 launch....
NuVasive launched ALIF Access, its first Maximum Access Surgery ALIF retractor for lateral and supine surgery approaches....
Spinal Resources announced successful clinical implantation of the first Swedge Pedicle Screw....
Studies demonstrated advantages of NuVasive's Porous PEEK interbody fusion devices vs. titanium-coated PEEK in impaction durability....
Amedica was issued a U.S. patent addressing Ceramic and/or Glass Materials and Related Methods....
Nanovis received FDA 510(k) clearance to market FortiCore® interbody fusion devices that feature a Nanosurface-enhanced porous titanium scaffold, intermolded with...
Study results demonstrate that RTI Surgical's Simmetry® Sacroiliac Joint Fusion system provided effective joint fixation, markedly reducing range of motion in the SI...
Life Spine received FDA 510(k) clearance to market the PLATEAU®-LO Insert and Rotate Spacer system for lumbar interbody fusion. ...
K2M commenced full launch of the next-generation YUKON OCT posterior fixation system, designed to support cervical sagittal balance in the occipito-cervico-thoracic regions....
CTL Medical received FDA 510(k) clearance for the MATISSE Ti-PEEK ACIF cage, featuring TiCro surface technology....
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