Medtronic Ave, Inc.
FDA 510(k) medical device clearances.
Top product codes for Medtronic Ave, Inc.
Recent clearances by Medtronic Ave, Inc.
- K032768 — MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L)
- K030633 — MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANT
- K030839 — MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)
- K022026 — MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)
- K014205 — MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE)
- K011080 — BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM
- K011817 — BRIDGE FX
- K002346 — WIRE, GUIDE, CATHETER, MODEL QSW1000
- K994141 — CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510; WIRE, GUIDE, CATHETER, MODEL QSW1000
- K000744 — MEDTRONIC AVE BRIDGE X3 STENT
- K993145 — MEDTRONIC AVE BRIDGE STENT
- K992569 — MEDTRONIC AVE BRIDGE STENT
- K992318 — MEDTRONIC AVE BRIDGE STENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.