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PMA de la FDA

Prosthesis, finger, constrained, metal/polymer

Número de PMA: P960053 · 2016-08-09

SolicitanteStryker Corporation
Fecha de decisión2016-08-09
Número PMAP960053
Código de productoKWG
Clase del dispositivoClase 3
Especialidad médicaO
Número de regulación21 CFR 8
Comité asesorOR

Resumen del dispositivo

Prosthesis, finger, constrained, metal/polymer is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2016-08-09. The device is classified under product code KWG. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Prosthesis, finger, constrained, metal/polymer?

Prosthesis, finger, constrained, metal/polymer is a medical device that received FDA 510(k) clearance on 2016-08-09. The listed applicant is Stryker Corporation.

When did Prosthesis, finger, constrained, metal/polymer receive FDA 510(k) clearance?

The clearance date for Prosthesis, finger, constrained, metal/polymer can be found in the official FDA records.

Who is the listed applicant for Prosthesis, finger, constrained, metal/polymer?

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

What is the FDA product code for Prosthesis, finger, constrained, metal/polymer?

The FDA product code for Prosthesis, finger, constrained, metal/polymer is KWG.

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Fuente oficial

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