# K152072: CrossRoads Screw System

- Pathway: 510(k) (Special)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Sep 23, 2015 after 58 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K962616 (1996). 91 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143039: CrossRoads Screw System, Orthodiscovery Group, LLC (D.B.A. Crossroads Extrem (2015) Summary page 4.
- K000080: Asnis Iii Cannulated Screw System, Howmedica Osteonics Corp. (2000) Summary page 4.
- K024060: Modification to Asnis Iii Cannulated Screw System, Howmedica Osteonics Corp. (2002) Summary page 4.

## Most influential descendants
- K191342: CrossRoads Screw System (2019), 0 descendants of its own
- K190722: TriMAX Implant System (2019), 0 descendants of its own
- K153638: Bicortical Fixation Screw & Washer Nut System (2016), 0 descendants of its own

## Indications for use
The CrossRoads Screw System is indicated for fracture repair and fixation, osteotomy, joint fusion, reconstruction and arthrodesis of bones appropriate for the size of the device.

Source page: https://510kreport.com/device/K152072
Methodology: https://510kreport.com/methodology