510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980290Substantially Equivalent

Iti Stent

Intratherapeutics, Inc., Saint Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980290 is the FDA 510(k) clearance record for ITI STENT, a class II device, cleared for Intratherapeutics, Inc. on under FDA product code FGE (Stents, Drains And Dilators For The Biliary Ducts). FDA records list 15 510(k) clearances for Intratherapeutics, Inc., from to . As of , FDA records show 12 recalls naming K980290.

Clearance record

Decision date
Received
(176 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
Intratherapeutics, Inc. 651 Campus Dr., Saint Paul 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