# K926232: Alta CFX Rod System

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Corp.
- Decided: Jun 17, 1993 after 188 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K960524: Alta CFX IM Rod System (1996), 2 descendants of its own
- K970257: Fixano D.S.S. (Double Sliding Screws) System for Osteosynthesis of Sub-Trochanterian Fractures (1997), 0 descendants of its own
- K963398: Alta Fully Threaded Cross-Locking Screws (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K926232
Methodology: https://510kreport.com/methodology