COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM
K-Number: K062264 · 2007-11-08
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Device Summary
Frequently Asked Questions
What is the COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM?
COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-08. The listed applicant is Medtronic Vascular. The 510(k) number is K062264.
When did COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM receive FDA 510(k) clearance?
COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM received FDA 510(k) clearance on 2007-11-08, under 510(k) number K062264.
Who is the listed applicant for COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM?
The FDA product code for COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM 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 Vascular 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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