4WEB Medical Receives FDA Clearance of Lateral Spine Truss

By Julie A. Vetalice

4WEB Medical received FDA 510(k) clearance to market its Lateral Spine Truss interbody fusion device.

The implants feature single-sterile packaging to ensure sterility, support operating room efficiencies and allow access to global markets that require sterile packaging.

In 4Q15, the company commenced U.S. launch of its Posterior Spine Truss system of interbody fusion devices, with applications including PLIF, TLIF and Oblique procedures.

Sources: 4WEB Medical, ORTHOWORLD Inc.

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory