FDA 510(k)

EXETER Centralizer, EXETER 2.5mm Plug

N.º K: K191414 · 2019-08-28

Fecha de decisión2019-08-28

Código de productoJDI

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

EXETER Centralizer, EXETER 2.5mm Plug is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Orthopaedics. It received FDA 510(k) clearance on 2019-08-28 under 510(k) number K191414. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the EXETER Centralizer, EXETER 2.5mm Plug?

EXETER Centralizer, EXETER 2.5mm Plug is a medical device that received FDA 510(k) clearance on 2019-08-28. The listed applicant is Stryker Orthopaedics. The 510(k) number is K191414.

When did EXETER Centralizer, EXETER 2.5mm Plug receive FDA 510(k) clearance?

EXETER Centralizer, EXETER 2.5mm Plug received FDA 510(k) clearance on 2019-08-28, under 510(k) number K191414.

Who is the listed applicant for EXETER Centralizer, EXETER 2.5mm Plug?

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

What is the FDA product code for EXETER Centralizer, EXETER 2.5mm Plug?

The FDA product code for EXETER Centralizer, EXETER 2.5mm Plug is JDI.

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Otros registros que enlistan a Stryker Orthopaedics como solicitante

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Dispositivos relacionados (Código: JDI)

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Fuente oficial

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