# K182087: DynaMesh-POSTERIOR

- Pathway: 510(k) (Traditional)
- Applicant: Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft
- Decided: Oct 31, 2018 after 90 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: 6 generations back to K962530 (1996). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161550: DynaMesh-VENTRAL, Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft (2016) Summary page 5.

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

Source page: https://510kreport.com/device/K182087
Methodology: https://510kreport.com/methodology