# K063671: Rebound HRD

- Pathway: 510(k) (Traditional)
- Applicant: Minnesota Medical Development, Inc.
- Decided: Aug 16, 2007 after 248 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: 1 generation back to K963141 (1996). 2 ancestors in all.
10 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060520: Vitamesh Macroporous PP Surgical Mesh, Proxy Biomedical, Ltd. (2006) Summary page 1.
- K963141: Kugel Hernia Patch, Douglas Bueschel (1996) Summary page 1.

## Most influential descendants
- K092726: Mesh GPS - Large, Small, SM, SM Small (2010), 7 descendants of its own
- K102766: Composix L/P Mesh with Echo PS Positioning System (2010), 6 descendants of its own
- K110820: Ventralight (TM) ST Mesh with Echo PS (TM) Positioning System (2011), 5 descendants of its own
- K122436: Composix L/P Mesh with Echo PS Positioning System Ventralight ST Mesh with Echo PS Positioning System (2012), 4 descendants of its own
- K080393: Modification to Rebound HRD (2008), 4 descendants of its own

## Indications for use
REBOUND HRDTM is intended to assist in the repair and/or reinforcement of hernia or other soft tissue defects where weakness exists and where the support of a nonabsorbable material is preferred.

Source page: https://510kreport.com/device/K063671
Methodology: https://510kreport.com/methodology