# K942370: Depuy Cemented Hip Prosthesis

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Nov 10, 1994 after 176 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.
38 later devices descend from it; 3 cite it directly.
0 of 39 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
- K013352: Summit Cemented Hip Prosthesis (2001), 36 descendants of its own
- K023453: Depuy Summit FX Cemented Hip Prosthesis (2002), 29 descendants of its own
- K170339: Summit Hip System (2018), 27 descendants of its own
- K193398: Summit DuoFix HA Coating (2020), 20 descendants of its own
- K202472: ACTIS Duofix Hip Prosthesis (2020), 15 descendants of its own

Source page: https://510kreport.com/device/K942370
Methodology: https://510kreport.com/methodology