Carbon22 Granted FDA 510(k) Clearance for Creed Cannulated Screw

By Julie A. Vetalice

Carbon22 Granted FDA 510(k) Clearance for Creed Cannulated Screw

Carbon22 received FDA 510(k) clearance to market the Creed™ Cannulated Screw System, a portfolio of ortholucent bone screws for foot and ankle surgery.

The multi-component Creed system features a proprietary hybrid screw composite, comprising a titanium core with an overmold of Solvay Zeniva® PEEK resin. While using medical imaging during and after surgery, the radiotranslucent properties of these headed and headless compression screws improve visualization of bony structures.

With a widened cannulation, Creed screws accept larger diameter k-wires and feature an enhanced self-drilling, self-tapping cutting screw tip that is unique to Carbon22.

Carbon22 is partnered exclusively with Solvay for the future development of medical-grade polymers.

Product Labels: Trauma Ankle/Foot/Toe

Tags: 510(k) Clearance, Regulatory