# K000232: Rotaglide + Modular Knee System with Fixed Meniscus

- Pathway: 510(k) (Special)
- Applicant: Corin USA
- Decided: Feb 25, 2000 after 29 days
- Product code: JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K013906: HLS Noetos System (2002), 3 descendants of its own
- K094013: HLS Kneetec System (2011), 1 descendant of its own
- K111970: Kneetec PFJ&HLS Kneetec Patellar Component (2012), 0 descendants of its own
- K032079: HLS Noetos System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K000232
Methodology: https://510kreport.com/methodology