# K010555: JAX

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew, Inc.
- Decided: Feb 25, 2003 after 729 days
- Product code: MQV (Filler, Bone Void, Calcium Compound)
- Device class: 2
- Regulation: 21 CFR 888.3045
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K041421: Name Bone Void Filler (2004), 4 descendants of its own
- K051722: Tricos T (2005), 3 descendants of its own
- K073571: Tricos T Resorbable Bone Substitute (2008), 2 descendants of its own
- K081717: Tricos a Resorbable Bone Substitute (2008), 0 descendants of its own
- K081721: Tricos a Resorbable Substitute (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K010555
Methodology: https://510kreport.com/methodology