Zimmer Biomet Gains 510(k) Clearance for Zyston Strut Open Titanium Interbody Spacer

By Julie A. Vetalice

Zimmer Biomet received FDA 510(k) clearance to market the Zyston® Strut Open Titanium Interbody Spacer, the company's first titanium spinal implant manufactured via 3D printing.

Zyston comprises a family of lumbar cages designed to enhance strength, graft capacity and visualization of the spacer, sized for a range of anatomies and surgical approaches. The system includes instruments for insertion, manipulation and implant removal.

Source: Zimmer Biomet

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory