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FDA 510(k)

Echo Intracranial Base Catheter

K-Number: K241637 · 2024-12-19

ApplicantStryker Neurovascular
Decision Date2024-12-19
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Echo Intracranial Base 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 2024-12-19 under 510(k) number K241637. 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 Echo Intracranial Base Catheter?

Echo Intracranial Base Catheter is a medical device that received FDA 510(k) clearance on 2024-12-19. The listed applicant is Stryker Neurovascular. The 510(k) number is K241637.

When did Echo Intracranial Base Catheter receive FDA 510(k) clearance?

Echo Intracranial Base Catheter received FDA 510(k) clearance on 2024-12-19, under 510(k) number K241637.

Who is the listed applicant for Echo Intracranial Base 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 Echo Intracranial Base Catheter?

The FDA product code for Echo Intracranial Base Catheter is QJP.

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.

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Other records listing Stryker Neurovascular 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.

K261889Trevo Trak 21 MicrocatheterPMA P170024Intracranial aneurysm flow diverterK253032AXS Lift Intracranial Base CatheterK252694Target Detachable CoilK251832InZone IST Detachment System; IZDS Connecting CablePMA P180031Intracranial coil-assist stent

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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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