# K033968: Hansson Pin System

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Osteonics Corp.
- Decided: Feb 20, 2004 after 60 days
- Product code: HTY (Pin, Fixation, Smooth)
- 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: 2 generations back to K760454 (1976). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K964893: Hansson Pin System, Osteonics Corp. (1997) Summary page 1.
- (no number) ASNIS II & III Cannulated Bone Screws: named in the summary without a submission number

## Most influential descendants
- K131591: Free Gliding Slipped Capital Femoral Epiphysis Screw (Scfe) (2013), 0 descendants of its own

## Indications for use
The Hansson Pin System is intended for use in the temporary stabilization of types of fractures of the proximal femur. The subject device is indicated for fixation of proximal femoral fractures including but not limited to: * Intracapsular fractures of the femoral neck such as Transcervical and Subcapital Neck Fractures * Basal Neck Fractures * Slipped Capital Femoral Epiphysis (in pediatric patients)

Source page: https://510kreport.com/device/K033968
Methodology: https://510kreport.com/methodology