FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

BRIDGE FX

K Number: K011817 · Decision Aug 22, 2001
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
13
Review Days
72

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Basic Information

Device Name
BRIDGE FX
K Number
K011817
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Medtronic Ave, Inc.
Date Received
June 11, 2001
Decision Date
August 22, 2001
Product Code
FGE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FGE Stents, Drains And Dilators For The Biliary Ducts

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FGE), ordered by most recent decision date.

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Other Clearances by Medtronic Ave, Inc.

K Number Device Name
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
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
Search all 13 clearances from Medtronic Ave, Inc. →