# K946371: Provident HP System

- Pathway: 510(k) (Traditional)
- Applicant: Stelkast Company
- Decided: Apr 5, 1995 after 120 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.
32 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K073068: Accin Hip System (2008), 28 descendants of its own
- K100445: Klassic HD Hip System (2010), 25 descendants of its own
- K143407: Klassic HD Hip System (2014), 16 descendants of its own
- K141972: Klassic HD Acetabular Insert with E-Link Poly (2014), 14 descendants of its own
- K163577: Ecofit® Hip System (2017), 9 descendants of its own

Source page: https://510kreport.com/device/K946371
Methodology: https://510kreport.com/methodology