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Medtronic CardioVascular

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Pioneer Plus Catheter PPlus 120 dual lumen device, inserted through a 6F introducer sheath recall (Z-0864-2011)Medtronic CardioVascular2011-01-06
Medtronic Racer Biliary Stent System, Model number XD518YF, UPC code 00721902758164 in a b recall (Z-1802-2010)Medtronic CardioVascular2010-06-14
Complete SE Biliary Stent System, SC5120L (5 mm x 12 mm), lot number 0000983799, UPC code recall (Z-0654-2010)Medtronic CardioVascular2010-01-19
Complete SE Biliary Stent System, SC680L (6 mm x 120 mm), lot number 0000983806, UPC code recall (Z-0655-2010)Medtronic CardioVascular2010-01-19
Medtronic COMPLETE SE Self Expanding Biliary Stent System, Model number SC760L, includes a recall (Z-0642-2009)Medtronic Cardiovascular2009-03-18
AneuRx AAAdvantage stent graft and the Xcelerant Delivery System with Hydro, Product numbe recall (Z-1918-2008)Medtronic CardioVascular2008-09-16
Medtronic brand AneuRx AAAdvantage Endovascular Stent Graft with the Xcelerant Delivery Sy recall (Z-0689-2008)Medtronic CardioVascular2008-04-08

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Every clearance here is in the API, with alerts when new ones post.