Camber Spine Gains FDA Clearance for ENZA-A Titanium ALIF
Camber Spine received FDA 510(k) clearance to market the ENZA-A Titanium Anterior Lumbar Interbody Fusion system....
Camber Spine received FDA 510(k) clearance to market the ENZA-A Titanium Anterior Lumbar Interbody Fusion system....
iOrthopedics has received patent awards and allowances for its Universally Expanding Cage, giving exclusive rights in the expandable interbody arena....
Medicrea obtained what is reported to be the first FDA 510(k) clearance to market patient-specific spinal cages....
K2M received FDA 510(k) clearance to market BACS® Patient-Specific devices. ...
NuVasive's SpineTRACK Registry reached a milestone of 10,000 patients enrolled since its inception in 2011. ...
Spinal Elements commenced full launch of the Clutch® interspinous process device for treatment of various posterior thoracolumbar pathologies....
Medacta announced FDA 510(k) clearance and launch of the MySpine Midline Cortical Pedicle Screw Placement Guide....
Implanet launched JAZZ Evo® for adult vertebral fusion. The device is the first in a new range of JAZZ® connectors....
Life Spine received FDA 510(k) clearance to market additional indications for the PRO-LINK® Ti Stand-Alone Cervical Spacer....
Wenzel Spine announced publication of a case series detailing endoscopic transforaminal decompression and fusion with the VariLift-LX system....
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