# K071673: Onc Solutions Marker, Models 001001 to 001012 and 001021 to 001032

- Pathway: 510(k) (Traditional)
- Applicant: Onc Solutions, Inc.
- Decided: Jul 18, 2007 after 29 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K874787 (1987). 11 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031206: Radiomed Soft Tissue Marker, Radiomed Corp. (2003) Summary page 1.
- K070305: Pre-Loaded Visicoil, Radiomed Corporation (2007) Summary page 1.
- (no number) 17G, 18G, 19G Introducer Needles manufactured by CP Medical: named in the summary without a submission number

## Most influential descendants
- K140823: Permanent Beacon Transponder/Soft Tissue Beacon Transponder (2014), 2 descendants of its own
- K170570: Anchored Beacon (R) transponder, Anchored transponder, Beacon Care Package - Lung (2018), 0 descendants of its own
- K152761: Permanent Beacon Transponder, Soft Tissue Beacon Transponder, Beacon Care Package - Soft Tissue (17G) (2015), 0 descendants of its own

## Indications for use
ONC Marker is indicated for use to radiographically mark soft tissue for future therapeutic procedures.

Source page: https://510kreport.com/device/K071673
Methodology: https://510kreport.com/methodology