Arthro Kinetics, Inc. is one of 25138 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arthro Kinetics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARTHRO KINETICS VESALIUS MR GENERATOR, MODELS 2004-2006, ENDOSCOPIC SPINE SYSTEM
2
Total
2
Cleared
0
Denied
Arthro Kinetics, Inc. has 2 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Arthro Kinetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arthro Kinetics, Inc.
2 devices