BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM
K-Number: K011080 · 2001-10-11
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Device Summary
Frequently Asked Questions
What is the BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM?
BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2001-10-11. The listed applicant is Medtronic Ave, Inc.. The 510(k) number is K011080.
When did BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM receive FDA 510(k) clearance?
BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM received FDA 510(k) clearance on 2001-10-11, under 510(k) number K011080.
Who is the listed applicant for BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM?
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 BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM?
The FDA product code for BRIDGE SE SELF-EXPANDING STENT DELIVERY 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 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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