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FDA 510(k)

AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter

K-Number: K200206 · 2020-02-27

ApplicantStryker Neurovascular
Decision Date2020-02-27
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2020-02-27 under 510(k) number K200206. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter?

AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter is a medical device that received FDA 510(k) clearance on 2020-02-27. The listed applicant is Stryker Neurovascular. The 510(k) number is K200206.

When did AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter receive FDA 510(k) clearance?

AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter received FDA 510(k) clearance on 2020-02-27, under 510(k) number K200206.

Who is the listed applicant for AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter?

The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter?

The FDA product code for AXS Vecta 71 Intermediate Catheter, AXS Vecta 74 Intermediate Catheter is QJP.

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Related Devices (Code: QJP)

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.

K260199SLIM MicrocatheterBalt USA, LLCK253901Millipede88 Access CatheterPerfuze, Ltd.K261889Trevo Trak 21 MicrocatheterStryker NeurovascularK261808ISAAC Neurovascular Navigation CatheterMicrovention Inc. d/b/a Terumo NeuroK261549BOBBY Balloon Guide CatheterMicroVention, Inc., d/b/a Terumo NeuroK253359Zenith Distal Access Long SheathSuzhou Zenith Vascular SciTech Limited

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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