# K073651: Neotract Anchor System

- Pathway: 510(k) (Traditional)
- Applicant: Neotract, Inc.
- Decided: Feb 1, 2008 after 37 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K003522 (2001). 2 ancestors in all.
2 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)
- K061700: Neotract Anchor, Neotract, Inc. (2006) Summary page 2.

## Most influential descendants
- 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

## Indications for use
The NeoTract Anchor System is intended for the approximation of soft tissue in open surgical procedures.

Source page: https://510kreport.com/device/K073651
Methodology: https://510kreport.com/methodology