NGMedical Granted FDA Clearance for AM Titanium Cervical Interbody BEE

By Julie A. Vetalice

NGMedical Granted FDA Clearance for AM Titanium Cervical Interbody BEE

NGMedical received FDA 510(k) clearance to market its additively manufactured titanium cervical BEE® cage.

The honeycomb structure of BEE supports bony ingrowth and demonstrates the reduced use of titanium minimizing risks of x-ray artefacts, while offering a very large graft space.

"This is an important step for NGMedical and allows us to start our active market presence in the USA. We are proud having received the FDA clearance based on the innovative design introduced to the OUS market in 2020. Our team did a great job in cooperation with MRC Global," said Nino Weiland, Operations Manager of NGMedical.

Product Labels: Cervical Spine, Spinal Fusion

Tags: 510(k) Clearance, Regulatory