Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
FDA product code NFA · 22 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.1250
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2001-06-01 – 2008-08-01
NFA
2008-08-01
NFA
2008-01-31
MODIFICATION TO PROXIS SYSTEM
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NFA
2007-01-19
SPIDERFX EMBOLIC PROTECTION DEVICE
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NFA
2006-10-20
TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03
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NFA
2006-09-13
PROXIS SYSTEM, MODEL EPS101
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NFA
2006-09-07
PROXIS SYSTEM
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NFA
2006-08-11
SPIDERX EMBOLIC PROTECTION DEVICE
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NFA
2006-08-11
FILTERWIRE EZ EMBOLIC PROTECTION SYSTEM (2.25 MM-3.5 MM)
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NFA
2006-07-11
TRIACTIV FX EMBOLIC PROTECTION SYSTEM
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NFA
2006-06-23
SPIDERX EMBOLIC PROTECTION DEVICE
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NFA
2006-04-10
FILTERWIRE EZ (2.25 MM - 3.5 MM) EMBOLIC PROTECTION SYSTEM, MODELS 20120-190, 20120-300
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NFA
2005-11-07
FILTERWIRE EZ EMBOLIC PROTECTION SYSTEM
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NFA
2005-06-08
EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150
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NFA
2005-03-23
TRIACTIV SYSTEM
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NFA
2004-08-06
FILTER WIRE EZ EMBOLIC PROTECTION SYSTEM AND EZ BENT TIP RETRIEVAL SHEATH
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NFA
2003-06-04
BOSTON SCIENTIFIC FILTERWIRE EX EMBOLIC
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NFA
2003-03-26
MODIFICATION TO EXPORT ASPIRATION CATHETER
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NFA
2003-01-24
GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
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NFA
2002-11-15
PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
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NFA
2002-10-29
EXPORT ASPIRATION CATHETER
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NFA
2002-01-25
MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM
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NFA
2001-06-01
PERCUSURGE GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
View details →No matching devices.
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