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Medtronic Vascular

208 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
THUNDER Extra Support Guidewire; Models: THNDR190J, THNDR190S, THNDR300J, THNDR300S Medtro recall (Z-0263-2014)Medtronic Vascular2013-11-15
ProVia CROSSING GUIDEWIRE; Models: 15PROV300HS, 3PROV180HS, 3PROV180SS, 3PROV300HS, 3PROV3 recall (Z-0264-2014)Medtronic Vascular2013-11-15
ATTAIN HYBRID Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain Hybrid guide recall (Z-0265-2014)Medtronic Vascular2013-11-15
COUGAR Steerable Guidewire; Models: LVCLS190J, LVCLS190S, LVCXT190J, LVCXT190S Medtronic g recall (Z-0266-2014)Medtronic Vascular2013-11-15
THUNDER Steerable Guidewire; Model: LVTNDR190S Medtronic guide wires are steerable guide w recall (Z-0267-2014)Medtronic Vascular2013-11-15
ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT recall (Z-0268-2014)Medtronic Vascular2013-11-15
Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactur recall (Z-0208-2007)Medtronic Vascular2006-11-22
Percutaneous Transluminal Coronary Angioplasty system in sterile pouch. recall (Z-1024-04)Medtronic Vascular2004-07-20
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Every clearance here is in the API, with alerts when new ones post.