# K062887: Modification to G2 Filter System-Femoral Delivery Kit, Model RF-310F

- Pathway: 510(k) (Special)
- Applicant: Bard Peripheral Vascular
- Decided: Oct 26, 2006 after 30 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
Longest line of descent: 2 generations back to K022236 (2002). 3 ancestors in all.
21 later devices descend from it; 1 cites it directly.
1 of 25 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050558: Modification to:  Recovery Filter System, Model RF-210F, C.R. Bard, Inc. (2005) Summary page 1.

## Most influential descendants
- K073090: Recovery G2 Filter System - Femoral Delivery Kit, Model RF-310F; Jugular/Subclavain Delivery Kit, Model RF-320J (2008), 20 descendants of its own
- K080668: G2 Express Filter System-Femoral (RF400F) and Jugular/Subclavian (RF400J) Delivery Kits (2008), 12 descendants of its own
- K082305: G2 Express Filter System - Femoral and Jugular/Subclavian Delivery Kits (2008), 11 descendants of its own
- K093659: Eclipse Filter System-Femoral Delivery Kit, Eclipse Filter System-Jugular/Subclavian Delivery Kit Model RF500F Model RF5 (2010), 8 descendants of its own
- K101431: Eclipse Filter System-Femoral and Jugular/Subclavian Delivery Kits (2010), 6 descendants of its own

## Indications for use
The G2 TM Filter System - Femoral Delivery Kit is indicated for use in the prevention of recurrent pulmonary embolism via permanent placement in the vena cava in the following situations: * Pulmonary thromboembolism when anticoagulants are contraindicated. * Failure of anticoagulant therapy for thromboembolic disease. * Emergency treatment following massive pulmonary embolism where anticipated benefits of conventional therapy are reduced. * Chronic, recurrent pulmonary embolism where anticoagulant therapy has failed or is contraindicated.

Source page: https://510kreport.com/device/K062887
Methodology: https://510kreport.com/methodology