# K062823: Aos Interstitial Templates, Needles & Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Alpha-Omega Services, Inc.
- Decided: May 29, 2007 after 251 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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) AOS Prostate Template: named in the summary without a submission number
- (no number) Rectal Template: named in the summary without a submission number
- (no number) GYN Template: named in the summary without a submission number
- (no number) AOS Template Needle: named in the summary without a submission number
- (no number) AOS Template Tip: named in the summary without a submission number
- (no number) AOS Implant Tube: named in the summary without a submission number
- (no number) AOS Implant Needle: named in the summary without a submission number
- (no number) AOS Retaining Button: named in the summary without a submission number

## Most influential descendants
- K233628: AOS Interstitial Templates, Needles, and Accessories (2024), 0 descendants of its own

## Indications for use
The purpose of AOS Interstitial Templates, Needles and Accessories is to provide and enclosed pathway for application of radioactive source(s) into the body or surface of the body for radiation therapy (brachytherapy).

Source page: https://510kreport.com/device/K062823
Methodology: https://510kreport.com/methodology