# K142528: AnthroBridge-Screw 25,30,35,40,45,50mm; AnthroBridge- Proximal Module 4.0,4.5,5.0mm

- Pathway: 510(k) (Traditional)
- Applicant: Agent Medical, LLC
- Decided: Dec 22, 2014 after 104 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: 5 generations back to K960385 (1996). 26 ancestors in all.
No later device cites it as a predicate yet.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024233: Kompressor Screw System, Kinetikos Medical, Inc. (2003) Summary page 4.
- K040356: Kompressor Screw System, Kinetikos Medical, Inc. (2004) Summary page 4.
- K130298: Biopro Kwick-Wire Universal Screw System, Biopro, Inc. (2013) Summary page 4.
- K122031: Nextra TI Hammertoe Correction System, Nextremity Solutions, LLC (2012) Summary page 4.
- K990804: Stayfuse, Pioneer Surgical Technology (1999) Summary page 4.
- K081149: Biopro GO-EZ Screw, Biopro, Inc. (2008) Summary page 4.

## Indications for use
The Agent Medical ArthroBridge System is intended to facilitate bone healing following reduction and fracture fixation of the small bones. The Agent Medical - ArthroBridge System is indicated for use for small bone fractures and osteotomy fixation and for distal phalangeal inter-digital fusion of the fingers and toes. The Agent Medical - ArthroBridge System is not for spinal use.

Source page: https://510kreport.com/device/K142528
Methodology: https://510kreport.com/methodology