# K100229: Ventrio Hernia Patch

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Apr 21, 2010 after 85 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: 3 generations back to K003323 (2001). 8 ancestors in all.
13 later devices descend from it; 6 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081777: Ventrio Hernia Patch, C.R. Bard, Inc. (2008)

## Most influential descendants
- K113229: Ventrio Light Hernia Patch with TRM Antimicrobial Coating (2012), 3 descendants of its own
- K101920: Ventrio ST Hernia Patch (2011), 3 descendants of its own
- K133223: Xenmatrix AB Surgical Graft (2014), 2 descendants of its own
- K190185: Phasix ST Mesh with Open Positioning System (2019), 1 descendant of its own
- K151177: XenMatrix AB Surgical Graft (2015), 1 descendant of its own

## Indications for use
The Ventrio Hernia Patch is indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

Source page: https://510kreport.com/device/K100229
Methodology: https://510kreport.com/methodology