# K001160: Versabond Bone Cement

- Pathway: 510(k) (Abbreviated)
- Applicant: Smith & Nephew, Inc.
- Decided: Dec 11, 2000 after 245 days
- Product code: LOD (Bone Cement)
- Device class: 2
- Regulation: 21 CFR 888.3027
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K033509: Modification to Versabond Bone Cement (2003), 1 descendant of its own
- K022688: Versabond AB Bone Cement (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K001160
Methodology: https://510kreport.com/methodology