# K070625: Pelvimesh / Hermesh 7

- Pathway: 510(k) (Traditional)
- Applicant: Marketing Solutions, Inc.
- Decided: Aug 1, 2007 after 148 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: 7 generations back to K921895 (1992). 40 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053424: Popmesh, Caldera Medical, Inc. (2006) Summary page 1.
- K041632: Minimesh Polypropylene Mesh, Mpathy Medical Devices, Ltd. (2004) Summary page 1.
- K973955: Herniamesh Surgical Meshes, Herniamesh (1998) Summary page 1.
- K043259: Bioblanket Surgical Mesh, Kensey Nash Corp. (2005) Summary page 1.

## Most influential descendants
- K081327: Relimesh (2008), 0 descendants of its own

## Indications for use
Hermesh 7 monofilament polypropylene mesh may be.used for repair of abdominal wall hernia, including inguinal, femoral, and incisional, in open or laparoscopic abdominal procedures.

Source page: https://510kreport.com/device/K070625
Methodology: https://510kreport.com/methodology