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FDA 510(k)

BRIDGE FX

K-Number: K011817 · 2001-08-22

ApplicantMedtronic Ave, Inc.
Decision Date2001-08-22
Product CodeFGE
Advisory CommitteeGU
DecisionUnknown

Device Summary

BRIDGE FX is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Ave, Inc.. It received FDA 510(k) clearance on 2001-08-22 under 510(k) number K011817. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BRIDGE FX?

BRIDGE FX is a medical device that received FDA 510(k) clearance on 2001-08-22. The listed applicant is Medtronic Ave, Inc.. The 510(k) number is K011817.

When did BRIDGE FX receive FDA 510(k) clearance?

BRIDGE FX received FDA 510(k) clearance on 2001-08-22, under 510(k) number K011817.

Who is the listed applicant for BRIDGE FX?

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 FX?

The FDA product code for BRIDGE FX is FGE.

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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.

K032768MEDTRONIC, INC. RACER BILIARY STENT SYSTEM (RACER), MODEL XD#YF(L)K030633MEDTRONIC AVE BRIDGE CONSTANT BILIARY STENT SYSTEM OR ('CONSTANTK030839MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)K022026MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS)K014205MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE)K011080BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM

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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.

K254179Drainage CatheterCanyon Medical, Inc.K262913Protégé™ EverFlex™ Self-expanding Peripheral Stent SystemMedtronic, Inc.K260835ARCHIMEDES Biodegradable Stent (Medium)Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.)K253393Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019 AG-5251-085519 AG-5251-088019 AG-5251-083021 AG-5251-085521 AG-5251-088021 AG-5251-083024 AG-5251-085524 AG-5251-088024 AG-5251-103018 AG-5251-105518 AG-5251-108018 AG-5251-103019 AG-5251-105519 AG-5251-108019 AG-5251-103021 AG-5251-105521 AG-5251-108021 AG-5251-103024 AG-5251-105524 AG-5251-108024 AG-5251-123018 AG-5251-125518 AG-5251-128018 AG-5251-123019 AG-5251-125519 AG-5251-128019Hangzhou AGS MedTech Co., Ltd.K253832Dilation Balloon CatheterMirco-Tech (Nanjing) Co., Ltd.K251658Endoflux™ Biliary & Pancreatic Stent SetsMedi-Globe GmbH

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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