MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)
K-Number: K022026 · 2002-07-19
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Device Summary
Frequently Asked Questions
What is the MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)?
MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) is a medical device that received FDA 510(k) clearance on 2002-07-19. The listed applicant is Medtronic Ave, Inc.. The 510(k) number is K022026.
When did MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) receive FDA 510(k) clearance?
MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) received FDA 510(k) clearance on 2002-07-19, under 510(k) number K022026.
Who is the listed applicant for MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)?
The FDA 510(k) record lists Medtronic Ave, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)?
The FDA product code for MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) is FGE.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medtronic Ave, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FGE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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