# K981051: Soft Tissue Patch Plus, Dualmesh Plus, Mycromesh Plus, Dualmesh Plus with Holes

- Pathway: 510(k) (Traditional)
- Applicant: W. L. Gore & Associates, Inc.
- Decided: Apr 15, 1998 after 28 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 K965038 (1997). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K965038: Gore-Tex Soft Tissue Patch Plus/Dualmesh Plus Biomaterial/Mycromesh Plus Biomaterial/Dualmesh Plus Biomaterial with Hole, W. L. Gore & Associates, Inc. (1997) Summary page 1.

## Most influential descendants
- K032168: Gore-Tex Dualmesh Emerge Plus Biomaterial (2003), 0 descendants of its own

## Indications for use
For use in the reconstruction of hernias and soft tissue deficiencies and for the temporary bridging of fascial defects.

Source page: https://510kreport.com/device/K981051
Methodology: https://510kreport.com/methodology