Walter Lorenz Surgical, Inc.

Walter Lorenz Surgical, Inc. — FDA 510(k) Submissions

Walter Lorenz Surgical, Inc. has submitted 56 FDA 510(k) premarket notifications since 1986, of which 56 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Bone, External Mandibular Fixator And/or Distractor, Plate, Fixation, Bone, Screw, Fixation, Bone, Marker, Radiographic, Implantable . Use the specialty filter in the sidebar to narrow results.