Camber Spine Exceeds 150th Implantation of ENZA Zero-Profile ALIF
Camber Spine Technologies has surpassed 150 implantations of its ENZAâ„¢ Zero-Profile ALIF device at one year following launch....
Camber Spine Technologies has surpassed 150 implantations of its ENZAâ„¢ Zero-Profile ALIF device at one year following launch....
CTL Medical received FDA 510(k) clearance to market the MATISSEâ„¢ titanium ACIF cage....
Medovex scheduled first cases in Germany for its DenerveXâ„¢ device to treat Facet Joint Syndrome....
Providence Medical Technology was granted regulatory approval in Australia for DTRAX® cervical fusion devices....
Vertera Spine received FDA 510(k) clearance to market the COALESCE™ interbody fusion device for ALIF, TLIF, PLIF and LLIF procedures. ...
Spinal Kinetics passed the milestone of a combined 50,000 implantations of its M6© artificial cervical and lumbar discs. ...
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...
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