LDR Receives FDA 510(k) Clearance for ROI-Lordotic Cervical Cage

Spinal Tech

Austin, Texas-based spinal device company LDR has received FDA 510(k) clearance for its ROI-C Lordotic Cervical Cage. The cage will belong to the company's stand-alone portfolio and complements the ROI-C anatomically shaped cage. The cage can be used with the company's VerteBRIDGE plating technology. The cage is designed to reduce the need for thick cervical plates that could contribute to dysphagia.

More Articles on Orthopedic Devices:

Johnson & Johnson Q1 Orthopedic Sales Flat

DePuy Spine Launches Pedicular Screw System for Spinal Fusions

Norwood Hospital Adopts MAKOplasty Partial Knee Resurfacing Technology


Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers