Frontier Medical Devices, Inc. is one of 18461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Frontier Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Frontier Medical Devices In-Line Orthopedic Cable Cerclage System, Frontier Medical Devices In-line Orthopedic Cable Cerclage System, Frontier Medical Devices Posterior Cable Screw System
5
Total
5
Cleared
0
Denied
Frontier Medical Devices, Inc. has 5 FDA 510(k) cleared medical devices. Based in Apple Valley, US.
Historical record: 5 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Frontier Medical Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Silver Pine Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Frontier Medical Devices, Inc.
5 devices
Cleared
Jan 13, 2016
Frontier Medical Devices In-Line Orthopedic Cable Cerclage System
Orthopedic
65d
Cleared
Oct 30, 2015
Frontier Medical Devices In-line Orthopedic Cable Cerclage System
Orthopedic
112d
Cleared
Aug 20, 2015
Frontier Medical Devices Posterior Cable Screw System
Orthopedic
92d
Cleared
Feb 26, 2015
Ancora LLC Interbody Fusion Device
Orthopedic
108d
Cleared
Nov 01, 2012
FRONTIER SADL INTERBODY FUSION DEVICE
Orthopedic
412d