# K953111: Corail

- Pathway: 510(k) (Traditional)
- Applicant: Landos, Inc.
- Decided: Dec 27, 1996 after 543 days
- Product code: LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3353
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
251 later devices descend from it; 10 cite it directly.
0 of 252 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K042992: Corail Amt Hip Prosthesis (2005), 168 descendants of its own
- K043079: Bicontact Hip System with U-Cap (2004), 166 descendants of its own
- K093472: Trinity Acetabular System (2010), 117 descendants of its own
- K110087: Corin Trinity Acetbular System with Hxlpe Liners (2011), 109 descendants of its own
- K060437: Excia Total Hip System with U-Cap (2006), 90 descendants of its own

Source page: https://510kreport.com/device/K953111
Methodology: https://510kreport.com/methodology