# K951508: Stainless Steel Greenfield Vena Cava Filter with 24F Introducer System

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Jun 22, 1995 after 80 days
- Product code: DTK (Filter, Intravascular, Cardiovascular)
- Device class: 2
- Regulation: 21 CFR 870.3375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K081410: Option Vena Cava Filter (2009), 6 descendants of its own
- K133243: Option Elite Vena Cava Filter System (2013), 2 descendants of its own
- K120402: Crux Vena Cava Filter System (2012), 2 descendants of its own
- K143405: Option (TM) ELITE Vena Cava Filter 100cm System (2015), 1 descendant of its own
- K122585: Crux Vena Cava Filter System (2013), 1 descendant of its own

Source page: https://510kreport.com/device/K951508
Methodology: https://510kreport.com/methodology