# K911052: Nexus (TM) Femoral Hip Stem

- Pathway: 510(k) (Traditional)
- Applicant: Dow Corning Wright
- Decided: Jun 17, 1991 after 101 days
- Product code: JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented)
- Device class: 2
- Regulation: 21 CFR 888.3350
- 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; 2 cite 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K240046: Ethylene Oxide Sterilization Supplier Change for MPO Hips (2024), 0 descendants of its own
- K113019: Profemur XM Wingless Distal Centralizer, Perfecta Distal Centralizer (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K911052
Methodology: https://510kreport.com/methodology