# K051179: EZ Plus Retrieval Sheath, Model 38899-150

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corp
- Decided: Jun 8, 2005 after 30 days
- Product code: NFA (Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K003992 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032884: Filter Wire EZ Embolic Protection System and EZ Bent Tip Retrieval Sheath, Boston Scientific Epi (2004) Summary page 1.

## Indications for use
The EZ Plus Retrieval Sheath is indicated for use with the Boston Scientific FilterWire EZTM Embolic Protection System as an alternative method for retrieval and/or redeployment of a deployed FilterWire EZ device. Reference the FilterWire EZ Embolic Protection System Instructions for Use for indications, warnings and precautions for the system.

Source page: https://510kreport.com/device/K051179
Methodology: https://510kreport.com/methodology