# K023210: Seedlinks, Models 70301, 70302, 70303

- Pathway: 510(k) (Traditional)
- Applicant: Sourcetech Medical, LLC
- Decided: Mar 28, 2003 after 183 days
- Product code: KXK (Source, Brachytherapy, Radionuclide)
- Device class: 2
- Regulation: 21 CFR 892.5730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K113210: Advantage-Strand/Advantage-Load Brachytherapy Kit (2012), 1 descendant of its own
- K242818: IsoSphere (2025), 0 descendants of its own

## Indications for use
The SeedLinksm are indicated for use in brachytherapy source spacing and linking in brachytherapy procedures.

Source page: https://510kreport.com/device/K023210
Methodology: https://510kreport.com/methodology