# K023293: Med-Tec Bellyboard, Models MT-Bba-01 & MT-Bba-02

- Pathway: 510(k) (Traditional)
- Applicant: Med-Tec,Inc.
- Decided: Dec 23, 2002 after 82 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
22 later devices descend from it; 2 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K060737: Sinmed Positioning Devices (2006), 17 descendants of its own
- K093738: Mri Patient Positioning Devices (2010), 14 descendants of its own
- K111340: Head and Neck Immobilization System, Body Immobilization System (2011), 13 descendants of its own
- K040773: Pelvis Bellyboard Plus Patient Positioning System (2004), 9 descendants of its own
- K142420: Patient Positioning Devices (2015), 7 descendants of its own

## Indications for use
The intended use of this device is to provide a cutout for displacement of the small bowel from the treatment area. The belly board can be used by it's self or with MED-TEC's HipFix system. The MED-TEC bellyboard is placed on the treatment table and has a cutout that aids in the displacement of the small bowel from the treatment area.

Source page: https://510kreport.com/device/K023293
Methodology: https://510kreport.com/methodology