# K161550: DynaMesh-VENTRAL

- Pathway: 510(k) (Traditional)
- Applicant: Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft
- Decided: Dec 22, 2016 after 202 days
- Product code: FTL (Mesh, Surgical, Polymeric)
- Device class: 2
- Regulation: 21 CFR 878.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K962530 (1996). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131530: Dynamesh -Cicat, Feg Textiltechnik Forschungs-Und Entwicklungsgesel (2013) Summary page 5.

## Most influential descendants
- K182087: DynaMesh-POSTERIOR (2018), 0 descendants of its own

## Indications for use
DynaMesh®-VENTRAL serves to support the tissue and stabilize the fascial structures of the abdominal wall. DynaMesh®-VENTRAL is indicated for repairing hernias in all current extraperitoneal surgical thecniques.

Source page: https://510kreport.com/device/K161550
Methodology: https://510kreport.com/methodology