# K060329: Endofast Reliant System

- Pathway: 510(k) (Traditional)
- Applicant: Endogun Medical Systems
- Decided: Sep 11, 2006 after 214 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 K931386 (1993). 14 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003949: Tacker, Model R65-933, A & A Medical, Inc. (2001) Summary page 2.
- K033636: Ams Large Pore Polypropylene Mesh, American Medical Systems, Inc. (2003) Summary page 2.

## Most influential descendants
- K080836: Modification to Endofast Reliant System (2008), 1 descendant of its own
- K130059: Endofast Reliant SCP, Endofast Reliant Lap (2013), 0 descendants of its own

## Indications for use
The EndoFast Reliant System is indicated for fixation of surgical mesh to tissues for tissue reinforcement during minimally invasive procedures

Source page: https://510kreport.com/device/K060329
Methodology: https://510kreport.com/methodology