CurvaFix’s Pelvic Fracture IM Implant Gets 510(k) Clearance

CurvaFix has received FDA’s 510(k) clearance for an updated version of its CurvaFix IM implant for smaller patients with fractures of the pelvis.

Based on surgeon feedback, the company redesigned the device for pelvic fractures in the narrow, curved pelvic corridors of smaller patients with high-impact trauma and fragility fracture.

The device, which is now available in 7.5mm and 9.5mm diameters, includes four internal cables that follow the bone’s natural curves and convert into a rigid state during implantation.