Medtronic Ave, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
- Regimes: 510(k) Registry: 510(k)
Bridge Se Self-Expanding Stent Delivery System Ref K011080
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Wire, Guide, Catheter, Model QSW1000 Ref K002346
Regimes: 510(k) Registry: 510(k)Bridge Fx Ref K011817
Regimes: 510(k) Registry: 510(k)Medtronic Ave Bridge X3 Stent Ref K000744
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Catheter, Intravascular Occluding, Temporary, Model Sol 3510; Wire, Guide, Catheter, Model QSW1000 Ref K994141
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Ave, Inc. have in the registry?
The registry currently lists 10 devices for Medtronic Ave, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Ave, Inc.'s devices?
Among its 10 most recently registered devices, Medtronic Ave, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Medtronic Ave, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Medtronic Ave, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Ave, Inc. in the registry?
The most recently registered devices listed for Medtronic Ave, Inc. include MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L), BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM, MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA) and MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANT.