# K895369: Voss Graft Marker

- Pathway: 510(k) (Traditional)
- Applicant: Voss Medical Products
- Decided: Sep 27, 1989 after 29 days
- Product code: KPK (Marker, Ostia, Aorto-Saphenous Vein)
- Device class: 2
- Regulation: 21 CFR 878.4650
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K050384: Kapp Bari-Ring, Model KS-BR-2005 (2006), 1 descendant of its own
- K072216: Kapp Bari-Ring Endoscopic Marker, Model K-9536 (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K895369
Methodology: https://510kreport.com/methodology