FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Advanix™ Pancreatic Stent and NaviFlex™ Rapid Exchange (RX) Pancreatic Delivery System and Pushers

K Number: K251291 · Decision Jul 3, 2025
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
58
Review Days
69

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Basic Information

Device Name
Advanix™ Pancreatic Stent and NaviFlex™ Rapid Exchange (RX) Pancreatic Delivery System and Pushers
K Number
K251291
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boston Scientific
Date Received
April 25, 2025
Decision Date
July 3, 2025
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

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