Spine

DePuy Synthes commenced U.S. launch of the CONCORDE LIFT Expandable Interbody, part of the UNLEASH MIS TLIF Procedural Solution....

FBC Device received its first FDA 510(k) clearance, granted for the FBC 921 ALIF interbody implant....

Results from an efficacy study of ReVivo Medical's spinal fusion technology demonstrated that loadsharing through elastic micro-motion accelerates bone formation and...

HAPPE Spine has formed to develop technology that supports construction of partial or fully porous hydroxyapatite-reinforced PEEK implants. ...

NuVasive commenced U.S. launch of MAGEC X, an extension of its MAGEC line to treat Early Onset Scoliosis. ...

K2M received FDA 510(k) clearance and CE Mark approval for the CAYMAN® United Plate....

Vallum received FDA 510(k) clearance to market a PEEK interbody fusion device with a PEEKplus® nanotextured surface created with proprietary Accelerated Neutral Atom Beam...

NuVasive introduced the Reline® MAS® Midline® cortical pedicle screw system for posterior fixation....

Life Spine commenced limited launch and announced first clinical use of the CENTRIC®-T Pedicle-Based Retractor for minimally invasive TLIF....

Cutting Edge Spine received FDA 510(k) clearance to market the EVOL ha-C cervical interbody system. ...