# K083467: Rebound HRDV

- Pathway: 510(k) (Special)
- Applicant: Minnesota Medical Development, Inc.
- Decided: Apr 23, 2009 after 150 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: 3 generations back to K963141 (1996). 4 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063671: Rebound HRD, Minnesota Medical Development, Inc. (2007) Summary page 1.
- K080393: Modification to Rebound HRD, Minnesota Medical Development, Inc. (2008) Summary page 1.

## Most influential descendants
- K143743: ECHO 2.0 LAP SYSTEM with VENTRALIGHT ST MESH (2015), 2 descendants of its own
- K170294: VENTRALIGHT ST Mesh with ECHO 2 Positioning System 11cm (4.5”) Circle, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 10cm x 15cm (4”x 6”) Ellipse,  VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm (6”) Circle, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm x 20cm (6”x8”) Ellipse, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm x 25cm (6”x10”) Oval (2017), 1 descendant of its own
- K182008: Phasix ST Mesh with Echo 2 Positioning System (2018), 0 descendants of its own

## Indications for use
REBOUND HRD® V 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/K083467
Methodology: https://510kreport.com/methodology