# K123066: Accumesh Deployment System

- Pathway: 510(k) (Special)
- Applicant: Covidien, LLC
- Decided: Oct 16, 2012 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: 3 generations back to K101218 (2010). 3 ancestors in all.
1 later device descends from it; 1 cites 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.
- K103269: Patchassist Large, Polytouch Medical, Ltd. (2010) Summary page 1.
- K121139: Accumesh Deployment System, Covidien, LLC (2012) Summary page 1.

## Most influential descendants
- K130782: Accumesh Deployment System (2013), 0 descendants of its own

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

Source page: https://510kreport.com/device/K123066
Methodology: https://510kreport.com/methodology