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PMA de la FDA

Prosthesis, finger, semi-constrained, metal/polymer

Número de PMA: P240020 · 2026-06-24

SolicitanteKeri Medical SA
Fecha de decisión2026-06-24
Número PMAP240020
Código de productoSFA
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Prosthesis, finger, semi-constrained, metal/polymer is the device name listed in this FDA 510(k) record. The listed applicant is Keri Medical SA. It received FDA 510(k) clearance on 2026-06-24. The device is classified under product code SFA. It was reviewed by the OR advisory panel.

Preguntas frecuentes

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

Prosthesis, finger, semi-constrained, metal/polymer is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Keri Medical SA.

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

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

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

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

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

The FDA product code for Prosthesis, finger, semi-constrained, metal/polymer is SFA.

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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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