Spine

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. ...

NuVasive is launching the XLIF® Lordotic Expandable interbody system for XLIF anterior column realignment, a minimally disruptive alternative to open...

Life Spine announced the first ASC procedures using robotic-assisted placement of CENTERLINE® Cortical Screws and PROLIFT® Expandable Spacers....

GS Medical commenced U.S. launch of the AnyPlus® Extended Tab system for minimally invasive pedicle screw placement. ...

Renovis Surgical Technologies received FDA 510(k) clearance to market Tesera® SA Hyperlordotic ALIF, a standalone interbody fusion system....

Globus Medical marked a milestone with successful implantation of >3,000 screws with ExcelsiusGPS® robotic guidance and navigation since late-2017 launch....