Medtronic Ave, Inc.
Medtronic Ave, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2003.
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.