Hoffmann LRF (Limb Reconstruction Frame) System

Hoffmann LRF (Limb Reconstruction Frame) System is an FDA 510(k)-cleared medical device (K153377) manufactured by Stryker GmbH. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 10, 2016. Regulation: 8.