# K002093: Atrium Lite Mesh

- Pathway: 510(k) (Special)
- Applicant: Atrium Medical Corp.
- Decided: Jul 24, 2000 after 13 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.
33 later devices descend from it; 4 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K043081: Gore Polypropylene Hernia Mesh (2004), 26 descendants of its own
- K052864: Tyrx Surgical Mesh, Model SMPC-0501 (2005), 25 descendants of its own
- K053656: Tyrx Antimicrobial Mesh (2006), 24 descendants of its own
- K063091: Pivit CRM (Tyrx Antimicrobial Pacemaker Pouch), Model CMRM-0601 (2008), 17 descendants of its own
- K130943: Aigis RX R PM/ Aigis RX R Icd (2013), 14 descendants of its own

Source page: https://510kreport.com/device/K002093
Methodology: https://510kreport.com/methodology