# K103269: Patchassist Large

- Pathway: 510(k) (Special)
- Applicant: Polytouch Medical, Ltd.
- Decided: Nov 23, 2010 after 19 days
- Product code: ORQ (Mesh, Surgical, Deployer)
- 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 K101218 (2010). 1 ancestor in all.
3 later devices descend from it; 3 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101218: Patchassist, Polytouch Medical, Ltd. (2010) Summary page 1.

## Most influential descendants
- K121139: Accumesh Deployment System (2012), 2 descendants of its own
- K123066: Accumesh Deployment System (2012), 1 descendant of its own
- K130782: Accumesh Deployment System (2013), 0 descendants of its own

## Indications for use
The PatchAssistTm device is intended to be used to facilitate the delivery of soft tissue prosthetics during the laparoscopic repair of soft tissue defects (e.g. hernia repair).

Source page: https://510kreport.com/device/K103269
Methodology: https://510kreport.com/methodology