# K002783: Fixion Interlocking Nail (Fixion IL Nail)

- Pathway: 510(k) (Traditional)
- Applicant: Disco-O-Tech Medical Technologies, Ltd.
- Decided: Dec 5, 2000 after 90 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.
61 later devices descend from it; 8 cite it directly.
0 of 62 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K010988: Fixion Interlocking Proximal Femoral Nailing System (2001), 59 descendants of its own
- K012967: Modification to Fixion Interlocking Proximal Femoral Intramedullary Nailing System (2001), 56 descendants of its own
- K021324: Fixion Intramedullary Nailing System (Fixion IM Nailing System) (2002), 54 descendants of its own
- K013449: Modification to Fixion Interlocking Intramedullary Nailing System (2001), 54 descendants of its own
- K023437: Fixion Interlocking Proximal Femur Intramedullary Nailing System (Fixion PF Nailing System), Fixion Intramedullary Nail (2002), 53 descendants of its own

Source page: https://510kreport.com/device/K002783
Methodology: https://510kreport.com/methodology