SpineGuard Scoops Up FDA Clearance for PediGuard

The FDA has granted 510(k) clearance to SpineGuard’s PediGuard Threaded dynamic surgical guidance device, the company announced Thursday.

The device can be used in open or minimally invasive procedures for pedicle screw insertion, and comes in several designs to accommodate surgeons’ preferences and patients’ anatomy, according to the company. — Anisa Jibrell