# K152136: Recovery Cone Removal System

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Feb 18, 2016 after 202 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K901502 (1990). 16 ancestors in all.
No later device cites it as a predicate yet.
2 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112185: Foursnare Vascular Retrieval Snare, Cook, Inc. (2011) Summary page 4.

## Indications for use
RC-15 Model: The Recovery Cone Removal System is intended for use to percutaneously remove the Recovery Filter, Recovery G2 Filter and G2 X Filter from the vena cava. FBRC Model: The Recovery Cone Removal System is intended for use to percutaneously remove the G2 X Filter, G2 Express Filter, G2 Filter and the Recovery Filter from the vena cava, or facilitate the retrieval of foreign objects from the peripheral vascular system.

Source page: https://510kreport.com/device/K152136
Methodology: https://510kreport.com/methodology