Conventus Orthopaedics Receives 510(k) Clearance for Distal Ulna and Proximal Ulna Systems

By Julie A. Vetalice

Conventus Orthopaedics received FDA 510(k) clearance to market its Conventus Cage™ DU (Distal Ulna) and PU (Proximal Ulna) systems for fracture repair.

The 3-dimensional Nitinol-based cage technology expands within bone to support stable fixation and prevent collapse of the repair.

These latest applications represent the fourth and fifth cleared indications for Conventus since 2013.

Sources: Conventus Orthopaedics, Inc.; ORTHOWORLD Inc.

Product Labels: Upper Extremity

Tags: 510(k) Clearance, Regulatory