# K092189: Pogo Screw

- Pathway: 510(k) (Special)
- Applicant: Fxdevices
- Decided: Sep 18, 2009 after 59 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: 4 generations back to K903810 (1990). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080649: Pogo Screw, Fxdevices (2008) Summary page 1.

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

## Indications for use
The POGO Screw is indicated for use in the general management of fractures and reconstructive surgery.

Source page: https://510kreport.com/device/K092189
Methodology: https://510kreport.com/methodology