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PMA de la FDA

Prosthesis, metatarsophalangeal joint cartilage replacement implant

Número de PMA: P150017 · 2021-12-10

SolicitanteCartiva, Inc.
Fecha de decisión2021-12-10
Número PMAP150017
Código de productoPNW
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Prosthesis, metatarsophalangeal joint cartilage replacement implant is the device name listed in this FDA 510(k) record. The listed applicant is Cartiva, Inc.. It received FDA 510(k) clearance on 2021-12-10. The device is classified under product code PNW. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Prosthesis, metatarsophalangeal joint cartilage replacement implant?

Prosthesis, metatarsophalangeal joint cartilage replacement implant is a medical device that received FDA 510(k) clearance on 2021-12-10. The listed applicant is Cartiva, Inc..

When did Prosthesis, metatarsophalangeal joint cartilage replacement implant receive FDA 510(k) clearance?

The clearance date for Prosthesis, metatarsophalangeal joint cartilage replacement implant can be found in the official FDA records.

Who is the listed applicant for Prosthesis, metatarsophalangeal joint cartilage replacement implant?

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

What is the FDA product code for Prosthesis, metatarsophalangeal joint cartilage replacement implant?

The FDA product code for Prosthesis, metatarsophalangeal joint cartilage replacement implant is PNW.

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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.

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