# K960642: Nancy Nail

- Pathway: 510(k) (Traditional)
- Applicant: Landos, Inc.
- Decided: May 17, 1996 after 93 days
- Product code: HTY (Pin, Fixation, Smooth)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
50 later devices descend from it; 1 cites it directly.
0 of 51 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
- K971783: Synthes Elastic Intramedullary Nail (Ein) System (1997), 49 descendants of its own
- K081452: Synthes (Usa) Stainless Steel Elastic Intramedullary Nail System (2008), 29 descendants of its own
- K032687: Ace Nancy Nail (2003), 17 descendants of its own
- K020885: Fassire-Duval Telescopic IM System (2003), 15 descendants of its own
- K082148: Synthes (Usa) Elastic Intramedullary Nail (Ein) End Cap, Line Extension (2008), 14 descendants of its own

Source page: https://510kreport.com/device/K960642
Methodology: https://510kreport.com/methodology