Spine

Medovex received its first 3 commercial orders for the DenerveX™ system from distributors in Germany, Italy and the U.K. ...

Meditech Spine received FDA 510(k) clearance for Talos® Lumbar PEEK IBF devices enhanced with hydroxyapatite....

SI-BONE received FDA 510(k) clearance and commenced full U.S. launch of the iFuse-3D™ Implant....

CMS issued a new ICD-10 code for a radiolucent porous interbody fusion device, supporting Vertera Spine’s COHERE cervical device. ...

Carevature Medical announced initial U.S. cases using the Dreal™ system for cervical spinal decompression....

Expanding Orthopedics announced CE Mark approval and launch of the FLXfit™15 interbody cage....

Medovex received CE Mark approval for the DenerveX™ system....

Prosidyan received FDA 510(k) clearance of FIBERGRAFT BG Putty for use in posterolateral spinal fusion. ...

Zimmer Biomet is recalling SpF® PLUS-Mini and SpF XL IIb Implantable Spinal Fusion Stimulators due to potential cytotoxicity issues that were...

K2M launched MESA 2 Cricket™ instrumentation, an enhancement to the MESA® 2 pedicle screw system. ...