# K900891: Modified Aml + Acetabular Cup Prosthesis

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Mar 12, 1990 after 13 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; 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K983491: Depuy Duraloc Acetabular Cup System-Enduron Liner (1998), 1 descendant of its own
- K191826: KeYi Total Hip System (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K900891
Methodology: https://510kreport.com/methodology