# K003270: Prostate Stepper Template Set, Model Part Number 189,065,189,066,189,067

- Pathway: 510(k) (Special)
- Applicant: Nucletron Corp.
- Decided: Dec 22, 2000 after 65 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
No predicates in its family tree.
6 later devices descend from it; 4 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K091230: HDR Prostate Template and Accessories (2009), 2 descendants of its own
- K170203: System, Applicator, Radionuclide, Remote Controlled (2017), 1 descendant of its own
- K201279: ASSISTO Universal Applicator Clamping Device (2020), 0 descendants of its own
- K082530: Applicators for Afterloading Brachytherapy (2008), 0 descendants of its own
- K031273: Ameritek Sure-Point HDR Needle Template (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K003270
Methodology: https://510kreport.com/methodology