# K121139: Accumesh Deployment System

- Pathway: 510(k) (Special)
- Applicant: Covidien, LLC
- Decided: May 2, 2012 after 16 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: 2 generations back to K101218 (2010). 2 ancestors in all.
2 later devices descend 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 2.
- K103269: Patchassist Large, Polytouch Medical, Ltd. (2010) Summary page 2.

## Most influential descendants
- K123066: Accumesh Deployment System (2012), 1 descendant of its own
- 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 the laparoscopic repair of soft tissue defects (e.g. hernia repair).

Source page: https://510kreport.com/device/K121139
Methodology: https://510kreport.com/methodology