# K041576: Sourcelink

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Jul 2, 2004 after 21 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.
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) SourceLink™ Brachytherapy Seeding Spacer Links: named in the summary without a submission number

## Most influential descendants
- K072296: Poiint of Care Stranding System, Mode 1004-00 (2007), 0 descendants of its own

## Indications for use
SourceLinkTM Connectors are indicated for use in seed spacing and linking in brachytherapy procedures.

Source page: https://510kreport.com/device/K041576
Methodology: https://510kreport.com/methodology