# K130298: Biopro Kwick-Wire Universal Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Biopro, Inc.
- Decided: Jun 18, 2013 after 131 days
- Product code: JDW (Pin, Fixation, Threaded)
- 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: 4 generations back to K962823 (1996). 15 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991649: Depuy Rockwood Clavicle Pin, Depuy, Inc. (1999) Summary page 1.
- K903258: Hagie Pin, Onyx Medical Corp. (1990) Summary page 1.
- K040356: Kompressor Screw System, Kinetikos Medical, Inc. (2004) Summary page 1.
- K031050: PCW Percutaneous Compression Wire, Millennium Medical Technologies, Inc. (2003) Summary page 1.

## Most influential descendants
- K142528: AnthroBridge-Screw 25,30,35,40,45,50mm; AnthroBridge- Proximal Module 4.0,4.5,5.0mm (2014), 0 descendants of its own
- K140875: Optossol Compression Device System (2014), 0 descendants of its own

## Indications for use
The BioPro Kwick-Wire™ Universal Screw System is indicated for use in the internal fixation of fractures, fusions and revisions. The system is intended for but not limited to hand surgery, orthopedic surgery and podiatric surgery — but is not intended for Spinal Use.

Source page: https://510kreport.com/device/K130298
Methodology: https://510kreport.com/methodology