# K002684: Composix E/X Mesh

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Oct 11, 2000 after 44 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.
44 later devices descend from it; 3 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Composix Mesh: named in the summary without a submission number
- (no number) SpermaTex Mesh: named in the summary without a submission number

## Most influential descendants
- K040868: Sepramesh IP Bioresorbable Barrier - Permanent Mesh (2004), 34 descendants of its own
- K053066: Sepramesh IP Bioresorbable Coating/Permanent Mesh (2005), 17 descendants of its own
- K063739: Sepramesh, Model 5959-1214 (2007), 16 descendants of its own
- K062915: Veritas Collagen Matrix (2006), 15 descendants of its own
- K061754: Bard Composite L/P Mesh (2006), 14 descendants of its own

## Indications for use
Reconstruction of soft tissue deficiencies, such as for the repair of hernias and chest wall defects.

Source page: https://510kreport.com/device/K002684
Methodology: https://510kreport.com/methodology