# K001932: Tornier Cement Restrictor

- Pathway: 510(k) (Special)
- Applicant: Tornier
- Decided: Jul 20, 2000 after 24 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K021765: Cement Restrictor, Small and Large (2002), 1 descendant of its own
- K210062: Mectaplug PE II (2021), 0 descendants of its own
- K061824: Tornier Cement Restrictor (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K001932
Methodology: https://510kreport.com/methodology