# K062639: Modification to Hexapod RT Couch Top

- Pathway: 510(k) (Special)
- Applicant: Medical Intelligence Medizintechnik-GmbH-An Elekta
- Decided: Sep 21, 2006 after 15 days
- Product code: JAI (Couch, Radiation Therapy, Powered)
- Device class: 2
- Regulation: 21 CFR 892.5770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) HexaPOD RT Couch Top: named in the summary without a submission number

## Indications for use
The intended use of the device is to support and aid in positioning a patient during radiation therapy.

Source page: https://510kreport.com/device/K062639
Methodology: https://510kreport.com/methodology