FDA 510(k)

Z5-TL

N.º K: K201712 · 2020-12-01

Fecha de decisión2020-12-01

Código de productoDZE

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Z5-TL is the device name listed in this FDA 510(k) record. The listed applicant is Z-Systems AG. It received FDA 510(k) clearance on 2020-12-01 under 510(k) number K201712. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Z5-TL?

Z5-TL is a medical device that received FDA 510(k) clearance on 2020-12-01. The listed applicant is Z-Systems AG. The 510(k) number is K201712.

When did Z5-TL receive FDA 510(k) clearance?

Z5-TL received FDA 510(k) clearance on 2020-12-01, under 510(k) number K201712.

Who is the listed applicant for Z5-TL?

The FDA 510(k) record lists Z-Systems AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Z5-TL?

The FDA product code for Z5-TL is DZE.

Otros registros que enlistan a Z-Systems AG como solicitante

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K201878ST-Z5 K200386Z5-BL K190243Z5-BL

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K261392TriActive Dental Implant SystemParagon Implant Mfg., LLC K260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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.