AI devices with FDA product code OOG — Knee Arthroplasty Implantation System

Product code OOG (“Knee Arthroplasty Implantation System” in openFDA) covers 1 device on the FDA AI-enabled list, from 1 company. Most are reviewed by the Orthopedic panel (1). The most recent decision was United Orthopedic Knee Patient Specific Instrumentation on December 20, 2023.