# K091230: HDR Prostate Template and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Photon Technologies Corporation
- Decided: Aug 12, 2009 after 107 days
- Product code: JAQ (System, Applicator, Radionuclide, Remote-Controlled)
- Device class: 2
- Regulation: 21 CFR 892.5700
- 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 K003270 (2000). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003270: Prostate Stepper Template Set, Model Part Number 189,065,189,066,189,067, Nucletron Corp. (2000) Summary page 1.

## Most influential descendants
- K170203: System, Applicator, Radionuclide, Remote Controlled (2017), 1 descendant of its own
- K201279: ASSISTO Universal Applicator Clamping Device (2020), 0 descendants of its own

## Indications for use
The HDR Prostate Template and Accessories are indicated for use as an accessory to commercially available high dose rate remote afterloading systems for prostate brachytherapy.

Source page: https://510kreport.com/device/K091230
Methodology: https://510kreport.com/methodology