K2M received FDA 510(k) clearance for expanded indications of its MESA® Mini and DENALI® Mini spinal systems for stabilization of the posterior cervical...
OrtoWay’s OrtoWell® Distractor instrument for spinal surgery may now be used in trauma or tumor removal applications. ...
Interventional Spine launched its next-generation Opticage® Lumbar Fusion line, including recent size additions and lordotic versions. ...
SpineSource commenced U.S. launch of the titanium alloy L-Varlock Lumbar Cage, reportedly the only expandable interbody that can adjust in situ...
Premia Spine launched the ProMIS™ spinal fixation system, which features a choice of screw placement techniques in a single instrument...
Implanet received FDA 510(k) clearance and CE Mark approval for Jazz Lock®, a band-shaped implant to treat degenerative spinal disorders,...
NuVasive is introducing its Integrated Global Alignment (iGA™) platform in the U.K. iGA packages procedural technology and tools as one platform to help...
Zyga Technology enrolled the 1st 4 patients in an expanded EVoluSIon Clinical Study evaluating long-term fusion and pain reduction in patients...
Renovis Surgical received FDA 510(k) clearance to market the Tesera™ SC porous titanium cervical interbody fusion system....
Results from 5-year clinical study comparing cervical total disc replacement (LDR’s Mobi-C) with anterior discectomy and fusion to treat 2-level degenerative disc...
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