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FDA 510(k)

INTRASTENT LD (LARGE DIAMETER) STENT

K-Number: K020528 · 2002-04-16

ApplicantSulzer Intratherapeutics, Inc.
Decision Date2002-04-16
Product CodeFGE
Advisory CommitteeGU
DecisionUnknown

Device Summary

INTRASTENT LD (LARGE DIAMETER) STENT is the device name listed in this FDA 510(k) record. The listed applicant is Sulzer Intratherapeutics, Inc.. It received FDA 510(k) clearance on 2002-04-16 under 510(k) number K020528. 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 INTRASTENT LD (LARGE DIAMETER) STENT?

INTRASTENT LD (LARGE DIAMETER) STENT is a medical device that received FDA 510(k) clearance on 2002-04-16. The listed applicant is Sulzer Intratherapeutics, Inc.. The 510(k) number is K020528.

When did INTRASTENT LD (LARGE DIAMETER) STENT receive FDA 510(k) clearance?

INTRASTENT LD (LARGE DIAMETER) STENT received FDA 510(k) clearance on 2002-04-16, under 510(k) number K020528.

Who is the listed applicant for INTRASTENT LD (LARGE DIAMETER) STENT?

The FDA 510(k) record lists Sulzer Intratherapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRASTENT LD (LARGE DIAMETER) STENT?

The FDA product code for INTRASTENT LD (LARGE DIAMETER) STENT is FGE.

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Other records listing Sulzer Intratherapeutics, 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.

K023243MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK021729MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK021563INTRACOIL SELF-EXPANDING PERIPHERAL STENTK014136MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK011806PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK012347PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY

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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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