LORENZ LACTOSORB LARYNGOTRACHEAL RECONSTRUCTION IMPLANTS

LORENZ LACTOSORB LARYNGOTRACHEAL RECONSTRUCTION IMPLANTS is an FDA 510(k)-cleared medical device (K012409) manufactured by Walter Lorenz Surgical, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 17, 2001. Regulation: 8.