# K912930: Interlocking Femoral Nailing System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Jan 13, 1992 after 192 days
- Product code: HSB (Rod, Fixation, Intramedullary And Accessories)
- Device class: 2
- Regulation: 21 CFR 888.3020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K091309: Revolution Femoral Intramedullary Nail System, Model Dgooxx (2009), 1 descendant of its own
- K100312: Distalock Femoral Intramedullary Nail System (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K912930
Methodology: https://510kreport.com/methodology