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

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

Cerapedics Study Results: i-FACTOR Bone Graft in Lumbar Posterolateral Spine

Study results indicate that Cerapedics' i-FACTOR Peptide Enhanced Bone Graft demonstrated a 50% fusion rate in lumbar posterolateral spine surgery patients vs. 20% fusion rate with allograft.

Providence Medical Technology Gains FDA Clearance for DTRAX Spinal System

Providence Medical Technology announced FDA 510(k) clearance to market its DTRAX® system for use in posterior cervical fusion.

Xtant Medical Expands Cervical Portfolio with First Porous Titanium Implant

Xtant Medical received FDA 510(k) clearance for its InTice-C Porous Titanium Cervical Interbody System.