Update regarding opportunities for orthopaedic surgeons to contribute to postmarket surveillance of potential safety issues for orthopaedic medical devices marketed in the United States
Arthroplast Today. 2017 Oct 16;3(4):205-206.
doi: 10.1016/j.artd.2017.09.003.
eCollection 2017 Dec.
1 Division of Orthopedic Devices, Center for Devices and Radiological Health, Office of Device Evaluation, U.S. Food and Drug Administration, Silver Spring, MD, USA.