# K002699: Parietex Composite (Pco) Mesh

- Pathway: 510(k) (Traditional)
- Applicant: Medical Device Consultants, Inc.
- Decided: Feb 15, 2001 after 169 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.
123 later devices descend from it; 8 cite it directly.
0 of 124 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K031955: Macropore Surgi-Wrap Mast Bioresorbable Sheet (2003), 76 descendants of its own
- K033376: Ugytex Mesh (2004), 70 descendants of its own
- K040998: Modification to Parietex Composite (Pco) Mesh (2004), 61 descendants of its own
- K050332: Surgi-Wrap Mast Bioresorbable Sheet (2005), 36 descendants of its own
- K050187: Parietex Composite Pco-OS and Pco-OB Meshes (2005), 31 descendants of its own

Source page: https://510kreport.com/device/K002699
Methodology: https://510kreport.com/methodology