Spinal Tech

Stryker received FDA 510(k) for the Tritanium PL Posterior Lumbar Cage for interbody fusions.

K2M reported revenue growth in 2015.

Cambridge, Mass.-based InVivo Therapeutics added University of Louisville (Ky.) Hospital as a clinical site for The INSPIRE study.

The FDA's approval of Medtronic's Specify SureScan MRI Surgical Leads completes the company's portfolio of full-body MRI conditional neurostimulation systems for chronic pain.

Zimmer Biomet completed the acquisition of Ortho Transmission's transcutaneous osseous integrated skeletal implant technology.

Belgrade, Mont.-based Xtant Medical received CE clearance for its Aranax Cervical Plating System and Irix-A stand alone anterior lumbar fusion device.

The global healthcare robotics market is expected to grow at a CAGR of more than 12 percent, according to Technavio.

A new study was published in The Spine Journal's February 2016 issue examining Titan Spine's surface technology.

The FDA cleared Captiva Spine's larger diameter screws within the TowerLOX MIS Pedicle Screw System and CapLOX II Pedicle Screws System.

OrthAlign received 510(k) clearance from the FDA to market its UniAlign system.