Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.)
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- Devices
- 1
What Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) makes
Medtronic manufactures the EverCross™ 0.035 OTW PTA Dilatation Catheter, a balloon catheter designed for percutaneous transluminal angioplasty (PTA) to dilate narrowed or obstructed blood vessels.
This device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is headquartered in the United States.
Catalogue
EverCrossTM 0.035 OTW PTA Dilatation Catheter Ref K190753
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) have in the registry?
The registry currently lists 1 device for Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.)'s devices?
Among its 1 most recently registered device, Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) in the registry?
The most recently registered devices listed for Medtronic, Inc. (Formerly D.B.A. Ev3, Inc. Covidien, LLC.) include EverCrossTM 0.035 OTW PTA Dilatation Catheter.