Spine

Zimmer Biomet received FDA approval for The Tether, a vertebral body tethering system that offers an alternative to fusion in the...

SeaSpine commenced limited launch of the Mariner® MIS Posterior Fixation System....

Spineology introduced Duo Angled Instrumentation to support access to the L4-L5 disc space when the iliac crest prevents collinear access....

Alphatec launched the InVictus MIS SingleStep K-wireless implant delivery system to limit potential complications from inadvertent K-wire advancement during pedicle screw placement....

Nexxt Spine received FDA 510(k) clearance for the NEXXT MATRIXX® Stand Alone Cervical interbody fusion device....

Bio2 Technologies enrolled the first patient in the Investigational Device Exemption trial of the Vitrium cervical interbody device....

Medicrea received FDA clearance to market the TULIP GENESIS top loading screw, the final element in its UNiD ASI spine...

Nanovis launched FortiCore® interbody fusion devices with a bioceramic nanotube-enhanced surface. ...

SeaSpine commenced limited launch of the Shoreline RT Cervical Interbody Implant featuring Reef Topography for increased surface area....

SeaSpine commenced limited launch of the Mariner® Outrigger® Revision System, an adjunct to Mariner Posterior Fixation....