# K003522: Salute

- Pathway: 510(k) (Traditional)
- Applicant: Onux Medical, Inc.
- Decided: Feb 13, 2001 after 90 days
- Product code: GDW (Staple, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4750
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K061700: Neotract Anchor (2006), 3 descendants of its own
- K073651: Neotract Anchor System (2008), 2 descendants of its own
- K101252: Neotract Anchor System Model: Ref 11208 (2010), 1 descendant of its own
- K102028: Neotract Anchor System Model TAS400 (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K003522
Methodology: https://510kreport.com/methodology