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Medtronic Vascular, Inc.

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Endurant / Endurant II 23mm and 25mm Bifurcated Stent Graft Systems Model Numbers: ETBF251 recall (Z-1543-2017)Medtronic Vascular, Inc.2017-03-15
Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP0 recall (Z-0243-2016)Medtronic Vascular, Inc.2015-11-06
FIBERNET Embolic Protection System: Recommended Vessel Diameter 3.5 0 5.0 mm, Maximum Guid recall (Z-1303-2014)Medtronic Vascular, Inc.2014-03-27
FIBERNET Embolic Protection System: Recommended Vessel Diameter 5.0 -6.0 mm, Maximum Guide recall (Z-1304-2014)Medtronic Vascular, Inc.2014-03-27
FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm, Maximum Guide recall (Z-1305-2014)Medtronic Vascular, Inc.2014-03-27
Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm; Stent length 34 mm recall (Z-0154-2014)Medtronic Vascular, Inc.2013-11-05
Valiant Thoracic Stent Graft with Captivia Delivery System, Talent Thoracic Stent Graft wi recall (Z-0083-2014)Medtronic Vascular, Inc.2013-10-25
NC Sprinter; Rapid Exchange Balloon Dilatation Catheter; Sterile; 2.25 mm; Model NCSP22512 recall (Z-2302-2013)Medtronic Vascular, Inc.2013-09-30
Talent Captivia Stent Graft System - FreeFlow configurations only. Model numbers affected recall (Z-1284-2012)Medtronic Vascular, Inc.2012-03-23

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