K2M Expands 3D-Printed MIS CASCADIA Lateral Interbody System

By Julie A. Vetalice

K2M received FDA 510(k) clearance for additional implant sizes of its CASCADIA™ Lateral Interbody System.

CASCADIA, part of K2M's minimally invasive spine portfolio, uses Lamellar 3D-printed Titanium Technology™ to create porous structures that support bony integration throughout the implant.

The CASCADIA family includes the CASCADIA TL, AN, AN Lordotic Oblique and Cervical Interbody systems.

Other device companies with lateral interbody offerings include Aurora Spine, ChoiseSpine, Life Spine, Medtronic, NuVasive, OsteoMed Spine, Tyber Medical, etc.

Sources: K2M, Inc.; FDA.gov; ORTHOWORLD Inc.

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory