# K060870: Avanza

- Pathway: 510(k) (Traditional)
- Applicant: Mds Nordion
- Decided: May 15, 2006 after 46 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
Longest line of descent: 1 generation back to K983678 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983678: Elekta Oncology Systems Precise Treatment Table, Elekta Instruments, Inc. (1999) Summary page 1.

## Indications for use
The Avanza patient positioning table is used as a universal patient support to accurately and reproducibly position patients for radiation therapy and simulation. The Avanza is used with THERATRON® Equinox TM units and is also adaptable to third party radiation therapy treatment devices.

Source page: https://510kreport.com/device/K060870
Methodology: https://510kreport.com/methodology