# K093196: Biomesh CA.B.S. 'Air Composite, Models: CABST1R05T, CABSAIRC7, CABSAIRC09

- Pathway: 510(k) (Abbreviated)
- Applicant: Cousin Biotech Sas
- Decided: Jun 25, 2010 after 259 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: 1 generation back to K021736 (2002). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072962: Cabs'air, Cousin Biotech Sas (2008) Summary page 1.
- K021736: Bard Ventralex Hernia Patch, Models 0010302, 0010301, C.R. Bard, Inc. (2002) Summary page 1.

## Indications for use
BIOMESH® CA.B.S.'Air® Composite is intended for use in all forms of hernia repair requiring reinforcement with nonabsorbable support material.

Source page: https://510kreport.com/device/K093196
Methodology: https://510kreport.com/methodology