FDA 510(k)

Target Detachable Coil

N.º K: K252694 · 2025-12-11

Fecha de decisión2025-12-11

Código de productoHCG

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Target Detachable Coil is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2025-12-11 under 510(k) number K252694. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Target Detachable Coil?

Target Detachable Coil is a medical device that received FDA 510(k) clearance on 2025-12-11. The listed applicant is Stryker Neurovascular. The 510(k) number is K252694.

When did Target Detachable Coil receive FDA 510(k) clearance?

Target Detachable Coil received FDA 510(k) clearance on 2025-12-11, under 510(k) number K252694.

Who is the listed applicant for Target Detachable Coil?

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 Target Detachable Coil?

The FDA product code for Target Detachable Coil is HCG.

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Otros registros que enlistan a Stryker Neurovascular como solicitante

K261889Trevo Trak 21 Microcatheter K253032AXS Lift Intracranial Base Catheter 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 K243593AXS Lift Intracranial Base Catheter K241637Echo Intracranial Base Catheter

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Dispositivos relacionados (Código: HCG)

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.