Stryker Gains FDA Clearance for SAHARA Lateral 3D Expandable Interbody
Stryker received FDA 510(k) clearance to market the SAHARA® Lateral 3D Expandable Interbody System featuring Lamellar 3D Titanium Technology....
Stryker received FDA 510(k) clearance to market the SAHARA® Lateral 3D Expandable Interbody System featuring Lamellar 3D Titanium Technology....
Life Spine and certain of its executives agreed to pay $6MM to resolve a civil healthcare fraud lawsuit alleging violations of...
Safe Orthopaedics received regulatory approval for SteriSpine™ LC lumbar and CC cervical cages in Japan....
Nanovis received the first FDA 510(k) clearance for a bioceramic nanotube surface that demonstrates FDA's requirements for nanotechnology....
Implanet was granted a patent in Japan for JAZZ Lock® technology, part of its JAZZ™ solutions platform to treat degenerative spine...
Alphatec launched IdentiTi™ porous titanium implants for lateral interbody fusion procedures....
CarboFix received FDA 510(k) clearance to market CarboClear® Carbon Fiber Vertebral Body Replacements....
Spineway obtained regulatory approval in Japan for its Mont Blanc minimally invasive surgical devices....
Zimmer Biomet launched the TrellOss™-TC Porous Titanium Interbody, completing its initial offering of porous titanium implants....
HD LifeSciences received a patent allowance notice addressing fluid channel technology employed in its interbody fusion devices. ...
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