Premia Spine Launches IDE Study of TOPS Spinal Arthroplasty Device
Premia Spine launched its U.S. pivotal Investigational Device Exemption study of the TOPS™ posterior arthroplasty device vs. traditional lumbar fusion....
Premia Spine launched its U.S. pivotal Investigational Device Exemption study of the TOPS™ posterior arthroplasty device vs. traditional lumbar fusion....
Medovex reported first human cases performed with the DenerveX™ system, used for the treatment of facet joint syndrome....
Emerging Implant Technologies received FDA 510(k) clearance for 3D-printed spinal interbody devices to address ALIF, PLIF, TLIF and cervical procedures....
Research indicates that Inspired Spine’s OLLIF procedure yielded substantial pain relief and minimal post-op complications in the trestment of adult degenerative...
SeaSpine commenced limited launch and announced initial case completion for the Skipjack™ Expandable Interbody System....
Pinnacle Spine was granted U.S. Patent No. 9,649,203, Methods of Post-Filling an Intervertebral Implant....
Xenco Medical expanded U.S. availability of the ASC CerviKit delivery and storage platform for disposable ACDFÂ systems....
Stryker received FDA 510(k) clearance for the MultiGen 2 RF Generator for radiofrequency ablation to treat facet joint pain. ...
Medtronic is recalling its KYPHON® Directional Bone Void Filler due to a misalignment issue that may cause injected cement to be...
Studies indicate that Providence Medical Technology’s tissue-sparing cervical fusion devices, CAVUX® Cervical and DTRAX® Expandable cages, yielded improvements in pain, with radiographic...
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