FDA 510(k)

Echo Intracranial Base Catheter

Número K: K241637 · 2024-12-19

Data da decisão2024-12-19

Código do produtoQJP

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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Outros registros que listam Stryker Neurovascular como candidato(a)

K261889Trevo Trak 21 Microcatheter K253032Cateter Intracraniano de Base AXS Lift K252694Target Detachable Coil K251832InZone IST Detachment System; IZDS Connecting Cable K242289Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27 Pre-Shaped Microcatheter, Excelsior XT-27 Flex Pre-Shaped Microcatheter K243593Cateter Intracraniano de Base AXS Lift

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Fonte oficial

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