# K070192: Atrium Prolite Ultra S Mesh

- Pathway: 510(k) (Special)
- Applicant: Atrium Medical Corp.
- Decided: Mar 8, 2007 after 45 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
No predicates in its family tree.
4 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)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K073579: Dynamesh-PP Standard, Model PP02NNNN, Dynamesh-PP Light, Model PP01NNNN (2008), 3 descendants of its own
- K131530: Dynamesh -Cicat (2013), 2 descendants of its own
- K161550: DynaMesh-VENTRAL (2016), 1 descendant of its own
- K182087: DynaMesh-POSTERIOR (2018), 0 descendants of its own

## Indications for use
Atrium ProLite Ultra S Mesh is indicated for use in hernia repair, chest wall reconstruction, traumatic or surgical wounds and other fascial surgical intervention procedures requiring reinforcement with a nonabsorbable supportive material.

Source page: https://510kreport.com/device/K070192
Methodology: https://510kreport.com/methodology