Centric Medical screw fixation system receives FDA 510(k) clearance — 3 things to know

Spinal Tech

Huntley, Ill.-based Centric Medical's Cannulated Screw Internal Fixation System received FDA 510(k) clearance for use in foot and ankle reconstruction procedures.

Here are three things to know:

 

1. Centric Medical develops surgical implants for the treatment of distal extremity pathology. Centric Medical is a division of Huntley-based Life Spine.

 

2. The internal fixation system is a streamlined multi-component system made of titanium alloy with a wide variety of diameters and lengths. The new options are specifically indicated for the forefoot and come in 2.0, 2.5, and 3.0 millimeter diameters with headed and headless options.

 

3. Centric Medical saw five 510(k) clearances in 2017 and sees a full cannulated screw selection as an integral step to a complete foot and ankle portfolio.

 

More articles on devices:

Smith & Nephew’s eCAP reduces readmissions 75% following total joint replacement surgery: 4 takeaways

1st spine surgeries successful with Jazz Lock in Brazil: 4 points

Catalyst OrthoScience adds George Rainey to board of directors — 4 things to know

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

 

Featured Webinars

Featured Whitepapers