Data / Medical devices / Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection (NFA): 3 FDA-registered makers in 2 countries
3 establishments in 2 countries are registered with the FDA to make Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection (product code NFA, Class 2, 21 CFR 870.1250). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 22 510(k) clearances under this code, the latest on August 1, 2008, and lists 2 recall events (0 Class I). FDA data exported November 3, 2026.
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- Product code
- NFA
- Device class
- 2
- Regulation
- 870.1250
- Medical specialty
- Cardiovascular
Makers by country
| Country | Makers |
|---|---|
| Costa Rica | 2 |
| United States | 1 |
Makers of Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Boston Scientific Corporation | La Aurora Heredia, Costa Rica | Specification developer | 1 | August 11, 2006 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | El Coyol Alajuela, Costa Rica | Manufacturer | 1 | August 11, 2006 | 0 | 0 | 0 | api.fda.gov |
| ev3, Inc. | Plymouth, MN, United States | Manufacturer | 1 | January 19, 2007 | 0 | 0 | 0 | api.fda.gov |
Updated August 1, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.