Empirical Spine Completes Portion of Enrollment for LimiFlex Clinical Trial
Empirical Spine completed enrollment in the investigational arm of its U.S. IDE trial of the LimiFlex Paraspinous Tension Band with decompression...
Empirical Spine completed enrollment in the investigational arm of its U.S. IDE trial of the LimiFlex Paraspinous Tension Band with decompression...
Life Spine was granted FDA 510(k) clearance to market the LONGBOW® Titanium Lateral Expandable Spacer....
SpineOvations began a clinical study of DiscSeal percutaneous injection for the treatment of low back pain....
NuVasive received FDA 510(k) clearance for expanded indications for the CoRoent Small Interlockâ„¢ system....
DePuy Synthes launched the SYMPHONY Occipito-Cervico-Thoracic System, expanding its offering for the treatment of conditions in the neck and upper spine....
4WEB Medical commenced limited launch of the Cervical Spine Truss System-Stand Aloneâ„¢ (CSTS-SA) implant....
Life Spine commenced limited launch of the CENTERLINE® Modular Thoracolumbar Spinal System, and announced initial surgeries. Full launch is slated...
CMS increased the Medicare Physician Fee Schedule for CPT® Code 27279, Arthrodesis Sacroiliac Joint, under which minimally invasive sacroiliac joint fusion procedures...
Two-year outcomes from Spineology's SCOUT trial of the OptiMesh® device revealed substantial improvements in low back pain and function scores at...
DiFusion received FDA 510(k)Â clearance for the Xiphos-ZF spinal interbody device made from ZFUZE biomaterial. Product launch will occur within 4Q19....
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