# K172785: Conquest FN

- Pathway: 510(k) (Special)
- Applicant: Smith & Nephew
- Decided: Dec 22, 2017 after 98 days
- Product code: JDO (Device, Fixation, Proximal Femoral, Implant)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K962616 (1996). 74 ancestors in all.
8 later devices descend from it; 2 cite it directly.
0 of 83 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152686: Conquest FN, Smith & Nephew (2016) Summary page 4.
- K111994: Smith & Nephew Cannulated Screws and Washers, Smith & Nephew, Inc. (2011) Summary page 5.
- K102057: Targon FN System, Aesculap Implant Systems, LLC (2010)
- K080649: Pogo Screw, Fxdevices (2008) Summary page 5.

## Most influential descendants
- 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
- K233017: TM Plating System (2023), 1 descendant of its own
- K261207: Exalta Proximal Tibia Plating System (2026), 0 descendants of its own
- K253713: Arthrex Variable Angle (VA) Proximal Tibia Plating System (2026), 0 descendants of its own

## Indications for use
The Smith & Nephew Conquest FN is indicated for displaced and undisplaced intracapsular femoral neck fractures.

Source page: https://510kreport.com/device/K172785
Methodology: https://510kreport.com/methodology