Subchondral Solutions Receives FDA Clearance for Fenestrated Cannulated Screws

By Julie A. Vetalice

Subchondral Solutions received FDA 510(k) clearance to market the fenestrated, cannulated S4 Screw System™ to treat osteochondral fractures.

S4 is the company's first FDA-cleared device in its platform that will address joint pain and damage with biomechanical and bioactive implants. The approach focuses on early biomechanical support for the entire bone/cartilage unit. Subchondral Solutions was established in California in 2014.

Source: Subchondral Solutions, Inc.


Product Labels: Upper Extremity, Lower Extremity

Tags: 510(k) Clearance, Regulatory