Genesis Fracture Care, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Genesis Fracture Care, Inc. has 5 FDA 510(k) cleared medical devices. Based in Clackamas, US.
Historical record: 5 cleared submissions from 2014 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Genesis Fracture Care, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Oct 23, 2017
G3™ Active Plate® Miniature System
Orthopedic
174d
Cleared
Apr 22, 2016
G3(TM) Active Plate(R) Small Fragment System
Orthopedic
46d
Cleared
Nov 24, 2015
G3¿ Active Plate® Large Fragment System
Orthopedic
106d
Cleared
Apr 30, 2015
G3 Active Plate Large Fragment System
Orthopedic
49d
Cleared
Nov 26, 2014
G3 Active Plate Large Fragment System
Orthopedic
48d