# K080649: Pogo Screw

- Pathway: 510(k) (Traditional)
- Applicant: Fxdevices
- Decided: Nov 25, 2008 after 263 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: 3 generations back to K903810 (1990). 11 ancestors in all.
15 later devices descend from it; 4 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060736: Smith & Nephew 6.5MM and 8.0MM Cannulated Screws, Smith & Nephew, Inc. (2006) Summary page 1.
- K071092: Asnis Micro Cannulated Screw, Howmedica Osteonics Corp. (2007) Summary page 1.

## Most influential descendants
- K152686: Conquest FN (2016), 12 descendants of its own
- K193029: Conquest FN (2020), 10 descendants of its own
- K172785: Conquest FN (2017), 8 descendants of its own
- K210837: Smith & Nephew Plates and Screws (2021), 7 descendants of its own
- K213126: Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws (2022), 2 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/K080649
Methodology: https://510kreport.com/methodology