ODi NA Gains FDA Clearance for Cannulated Compression Device

Orthopedic Designs North America, Inc. (ODi) was granted FDA 510(k) clearance to market their Cannulated Compression Device System (CCD).

This device is the first modular cannulated screw which utilizes ODi’s Talon™ Technology to treat both small and large bone fractures. This system reportedly offers five times the compression as compared...

document icon

You are out of free articles for this month

Subscribe as a Guest for $0 and unlock a total of 5 articles per month.

You are out of five articles for this month

Subscribe as an Executive Member for access to unlimited articles, THE ORTHOPAEDIC INDUSTRY ANNUAL REPORT and more.

JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



Contact Us

0