Crossroads Extremity Systems, LLC - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Crossroads Extremity Systems, LLC has 13 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Last cleared in 2023. Active since 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Crossroads Extremity Systems, LLC
13 devices
Cleared
Mar 30, 2023
MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System,...
Orthopedic
149d
Cleared
Apr 15, 2022
FootHold System
Orthopedic
28d
Cleared
Dec 30, 2020
CrossRoads Tray System
General Hospital
141d
Cleared
Apr 12, 2019
MIS Bunion Plating System
Orthopedic
29d
Cleared
Feb 19, 2019
MIS Bunion System
Orthopedic
222d
Cleared
Aug 09, 2018
MotoCLIP/HiMAX Step Staple Implant System
Orthopedic
28d
Cleared
Jun 29, 2018
MotoCLIP/HiMAX Implant System
Orthopedic
30d
Cleared
Feb 12, 2018
MotoBAND CP Implant System
Orthopedic
70d
Cleared
May 03, 2016
STROPP (Single Tunnel Repair of Plantar Plate)
Orthopedic
105d
Cleared
Apr 22, 2016
MotoBand(TM) CP Implant System
Orthopedic
78d
Cleared
Dec 11, 2015
MotoBand¿ CP Implant System
Orthopedic
119d
Cleared
Sep 23, 2015
CrossRoads Screw System
Orthopedic
58d
Cleared
Sep 04, 2015
CrossTIE Intraosseous Fixation System
Orthopedic
114d