Xtant Medical Expands Cervical Portfolio with First Porous Titanium Implant

By Julie A. Vetalice

Xtant Medical gained FDA 510(k) clearance for its InTice™-C Porous Titanium Cervical Interbody System. InTice-C uses OsteoSync Ti, a highly porous titanium scaffold material that more closely resembles the bioscaffold of cancellous bone.

InTice-C is also cleared for use with Xtant's proprietary allograft lines, including OsteoSponge®, 3Demin® Cortical Fibers, and OsteoVive™ viable cell allograft.

This is Xtant’s first spinal implant to use porous titanium.

Source: Xtant Medical Holdings, Inc.

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory