Spine

Zyga Technology announced the issuance of U.S. Patent No. 9,662,124, relating to the design of the SImmetry Decorticator®. ...

K2M introduced SAHARA™ AL, the company’s first expandable interbody product....

Medicrea received FDA 510(k) clearance and performed first surgeries with PASS® TULIP top-loading fixation....

Medicrea received FDA 510(k) clearance for UNiD™ HUB, a data-driven digital portal that employs Adaptive Spine Intelligence for surgical planning....

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....