ODi NA Gains FDA Clearance for Cannulated Compression Device

By Julie A. Vetalice

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 to the market leader.

Orthopedic Designs North America, Inc. was established to invent, develop, manufacture and market improved fixation products for the orthopedic community. In keeping with this charter, ODi offers new developments in orthopedic surgery encompassing its patented process: Talon™ Technology. This technology provides deployable, integral anchors which enhance fixation, compression and rotational stability.

Source: Orthopedic Designs North America

 

Product Labels: Trauma Ankle/Foot/Toe

Tags: 510(k) Clearance, Regulatory