# K081739: 2-Port Through-the-Peg (TTP) Jejunostomy Tube Kit

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Dec 3, 2008 after 167 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- 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 K971906 (1997). 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)
- K072476: Through-the-Peg (TTP) Jejunostomy Tube Kit, Boston Scientific Corporation (2007) Summary page 1.

## Most influential descendants
- K133096: Abb Vie J (2014), 1 descendant of its own
- K142816: AbbVie J (2015), 0 descendants of its own

## Indications for use
The EndoVive Two-Port Through The PEG (TTP) Jejunal Feeding Tube (J-Tube) Kit is intended to provide enteral access for decompression and delivery of nutrition and/or medication.

Source page: https://510kreport.com/device/K081739
Methodology: https://510kreport.com/methodology