# K932222: SLT Femoral Head

- Pathway: 510(k) (Traditional)
- Applicant: Dow Corning Wright
- Decided: May 27, 1994 after 385 days
- Product code: LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3353
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 2 cite it directly.
0 of 10 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
- K161520: ELEOS Limb Salvage System (2016), 6 descendants of its own
- K203090: ELEOS Limb Salvage System featuring BIOGRIP (2020), 1 descendant of its own
- K173898: MicroPort Orthopedics Total Hip Systems MR Labeling (2018), 1 descendant of its own
- K253066: ELEOS™ with NanoCept® Technology Limb Salvage System (2026), 0 descendants of its own
- K252920: ELEOS™ Limb Salvage System with NanoCept® Technology (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K932222
Methodology: https://510kreport.com/methodology