# K130782: Accumesh Deployment System

- Pathway: 510(k) (Special)
- Applicant: Covidien, LLC
- Decided: Apr 5, 2013 after 15 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: 4 generations back to K101218 (2010). 4 ancestors in all.
No later device cites it as a predicate yet.
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.
- K103269: Patchassist Large, Polytouch Medical, Ltd. (2010) Summary page 2.
- K123066: Accumesh Deployment System, Covidien, LLC (2012) Summary page 1.

## Indications for use
The AccuMesh Positioning System 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/K130782
Methodology: https://510kreport.com/methodology