# K072476: Through-the-Peg (TTP) Jejunostomy Tube Kit

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corporation
- Decided: Dec 14, 2007 after 101 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: 1 generation back to K971906 (1997). 1 ancestor in all.
4 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971906: Jejenostomy Feeding Tube, Boston Scientific Corp (1997) Summary page 1.

## Cited in the summary but kept off the family tree
- K042303: Vitros Immunodiagnostic Products Anti-HBS Controls, Ortho-Clinical Diagnostics (2004). Our reading of the summary gave K042303, FDA’s number for Vitros Immunodiagnostic Products Anti-HBS Controls (Ortho-Clinical Diagnostics). Its FDA name has none of the distinctive words the summary uses for the device it names, “Nasal Jejunal Feeding Tube, Nasal Feeding Tube with Flaps”. Kept off the family tree. Summary page 1.

## Most influential descendants
- K081739: 2-Port Through-the-Peg (TTP) Jejunostomy Tube Kit (2008), 2 descendants of its own
- K133096: Abb Vie J (2014), 1 descendant of its own
- K142816: AbbVie J (2015), 0 descendants of its own
- K091340: Through the -Peg (TTP) Jejunal Feeding Tube Kit, Model M00566320,M00566330, M00566340, M00566350 (2009), 0 descendants of its own

## Indications for use
The TTP Jejunostomy Tube Kit is intended to provide enteral access for decompression and delivery of nutrition and/or medication.

Source page: https://510kreport.com/device/K072476
Methodology: https://510kreport.com/methodology