FDA 510(k)

Meril-Bonewax

N.º K: K200452 · 2023-03-27

SolicitanteM/s. Meril Endo Surgery Private Limited.

Fecha de decisión2023-03-27

Código de productoMTJ

DecisiónSubstantially Equivalent

Resumen del dispositivo

Meril-Bonewax is the device name listed in this FDA 510(k) record. The listed applicant is M/s. Meril Endo Surgery Private Limited.. It received FDA 510(k) clearance on 2023-03-27 under 510(k) number K200452. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Meril-Bonewax?

Meril-Bonewax is a medical device that received FDA 510(k) clearance on 2023-03-27. The listed applicant is M/s. Meril Endo Surgery Private Limited.. The 510(k) number is K200452.

When did Meril-Bonewax receive FDA 510(k) clearance?

Meril-Bonewax received FDA 510(k) clearance on 2023-03-27, under 510(k) number K200452.

Who is the listed applicant for Meril-Bonewax?

The FDA 510(k) record lists M/s. Meril Endo Surgery Private Limited. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Meril-Bonewax?

The FDA product code for Meril-Bonewax is MTJ.

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Otros registros que enlistan a M/s. Meril Endo Surgery Private Limited. como solicitante

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Ver todos los 11 dispositivos →

Dispositivos relacionados (Código: MTJ)

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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.