Crossroads Extremity Systems, LLC
Crossroads Extremity Systems, LLC holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2023, with 2 FDA device recalls on record.
Top product codes for Crossroads Extremity Systems, LLC
FDA recalls by Crossroads Extremity Systems, LLC
- Z-0212-2020 — MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm
- Z-1487-2017 — MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Crossroads Extremity Systems, LLC
- K223342 — MotoBAND CP Implant System: DynaBunion 4D Minimal-incision Bunion System, DynaMET Lesser TMT Fusion System
- K220797 — FootHold System
- K202268 — CrossRoads Tray System
- K190658 — MIS Bunion Plating System
- K181872 — MIS Bunion System
- K181866 — MotoCLIP/HiMAX Step Staple Implant System
- K181410 — MotoCLIP/HiMAX Implant System
- K173710 — MotoBAND CP Implant System
- K160118 — STROPP (Single Tunnel Repair of Plantar Plate)
- K160300 — MotoBand(TM) CP Implant System
- K152306 — MotoBand¿ CP Implant System
- K152072 — CrossRoads Screw System
- K151270 — CrossTIE Intraosseous Fixation System
Data sourced from openFDA. This site is unofficial and independent of the FDA.