510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K030839Unknown

Medtronic Ave Bridge Aurora Biliary Stent System (Aurora)

Medtronic, Inc., Santa Rosa CA / Special, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030839 is the FDA 510(k) clearance record for MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA), a class II device, cleared for Medtronic Ave, Inc. on under FDA product code FGE (Stents, Drains And Dilators For The Biliary Ducts). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K030839.

Clearance record

Decision date
Received
(74 days to decision)
Product code
FGE Stents, Drains And Dilators For The Biliary Ducts
Regulation
21 CFR 876.5010
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medtronic Ave, Inc. 3576 Unocal Pl., Santa Rosa CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FGE

Trailing 12 months
10 clearances under product code FGE in the twelve months to November 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FGE, trailing twelve months
MonthClearances
December 20252
January 20260
February 20260
March 20262
April 20262
May 20260
June 20261
July 20261
August 20260
September 20262
October 20260
November 20260