510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K923993Substantially Equivalent

Wallstent Biliary Endoprotheses

Schneider U.S. Stent Div., Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923993 is the FDA 510(k) clearance record for WALLSTENT BILIARY ENDOPROTHESES, a class II device, cleared for Schneider U.S. Stent Div. on under FDA product code FGE (Stents, Drains And Dilators For The Biliary Ducts). FDA records list 3 510(k) clearances for Schneider U.S. Stent Div., from to . As of , FDA records show no recalls naming K923993.

Clearance record

Decision date
Received
(781 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
Schneider U.S. Stent Div. 5905 Nathan Ln., Plymouth MN
510(k) summary
Summary
Third party review
No

Clearances, product code FGE

Trailing 12 months
10 clearances under product code FGE in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FGE, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20262
April 20262
May 20260
June 20261
July 20261
August 20260
September 20262
October 20260