Spine

Spineology received FDA 510(k) clearance to market the Rampart™ Duo™ Interbody Fusion System, reportedly the first device to combine PEEK, titanium and...

Spine Wave will commence full launch of the Velocity® P Expandable Interbody Device system in mid-November....

The North American Spine Society/NASS issued first of its kind coverage recommendations for electrical bone growth stimulators as an adjunct to spinal fusion, supporting use of...

SIGNUS Medizintechnik announced FDA 510(k) clearance to market the DIPLOMAT® pedicle screw system. ...

Vertera Spine announced initial successful outcomes using the COHERE® Cervical Interbody Fusion device. ...

DeGen Medical introduced the Latitude-C™ Porous Ti Cervical Interbody Spacer....

Spinal Elements announced initial procedures using Katana™, its minimally invasive lateral system....

Medicrea received FDA 510(k) clearances for its PASS® XS posterior fixation and LigaPASS® XS band connector components, designed to address spinal deformities...

Paradigm BioDevices completed its 25,000th case with the QuickDraw MIS Bone Harvester™. A single-use, sterile version of the system is slated...

Randomized study results indicate that Safe Orthopaedics’ single-use spine surgical instruments yielded an 80% decrease in pre- and post-operative times....