FDA 510(k)

CoCr Head

N.º K: K211047 · 2023-01-10

Fecha de decisión2023-01-10

Código de productoLPH

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

CoCr Head is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer GmbH. It received FDA 510(k) clearance on 2023-01-10 under 510(k) number K211047. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CoCr Head?

CoCr Head is a medical device that received FDA 510(k) clearance on 2023-01-10. The listed applicant is Zimmer GmbH. The 510(k) number is K211047.

When did CoCr Head receive FDA 510(k) clearance?

CoCr Head received FDA 510(k) clearance on 2023-01-10, under 510(k) number K211047.

Who is the listed applicant for CoCr Head?

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

What is the FDA product code for CoCr Head?

The FDA product code for CoCr Head is LPH.

Otros registros que enlistan a Zimmer GmbH 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.

K200814Sistema de Uñas Naturales Affixus(R) Humeral Nail(R)K200112Zimmer Hip Joint Replacement K193099Sistema de Hombro Anatómico K193050Esbocado femoral Alloclassic Zweymuller SL, Esbocado femoral desviado Alloclassic Zweymuller SL K193030Avenir Muller Stem, Avenir Cemented Hip Stem K192236Fitmore Hip Stem

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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.