# K130613: Cannulated Screw and Kirschner (Kwire) System

- Pathway: 510(k) (Traditional)
- Applicant: Laura Cattabriga
- Decided: Jan 22, 2014 after 321 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: 7 generations back to K761228 (1976). 41 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071035: Ifs Bone Fixation Devices, Internal Fixation Systems, Inc. (2007) Summary page 2.
- K061620: Ifs Cannulated Bone Screw, Internal Fixation Systems, Inc. (2006) Summary page 2.

## Most influential descendants
- K252758: Cannulated Screw and Kirschner (K wire) System (2025), 0 descendants of its own

## Indications for use
The Intended Use of the Cannulated Screw and Kirschner (Kwire) System is for the treatment and fixation of bone fractures and osteoitomies of various bones including the acetabulum, pelvis, humerus, radius, ulna, femur, tibia, phalanges, carpals, metacarpals, tarsals, metatarsals and fibula

Source page: https://510kreport.com/device/K130613
Methodology: https://510kreport.com/methodology