Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Crossroads Extremity Systems with 19 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Jan 6, 2026: TRILEAP Plating System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 6, 2026 | TRILEAP Plating SystemK253178 · HRS | 510(k) clearances |
| Jul 16, 2024 | CrossRoads Modular Tray SystemK241050 · KCT | 510(k) clearances |
| Sep 29, 2023 | TriLEAP Plating SystemK230591 · HRS | 510(k) clearances |
| Mar 30, 2023 | MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System, DynaMET™ Lesser TMT Fusion SystemK223342 · HRS | 510(k) clearances |
| Apr 15, 2022 | FootHold SystemK220797 · MBI | 510(k) clearances |
| Dec 30, 2020 | CrossRoads Tray SystemK202268 · KCT | 510(k) clearances |
| Jan 10, 2020 | MotoBAND CP Implant SystemK193452 · HRS | 510(k) clearances |
| Sep 19, 2019 | MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mmClass II · Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw. | Device recalls |
| Aug 19, 2019 | CrossRoads Screw SystemK191342 · HWC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
