FDA 510(k)

Bendini Cloud Application

Номер K: K233706 · 2024-08-02

ЗаявительNuvasive

Дата решения2024-08-02

Код продуктаOLO

Консультативный комитетNE

РешениеSubstantially Equivalent

Описание устройства

Bendini Cloud Application is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive. It received FDA 510(k) clearance on 2024-08-02 under 510(k) number K233706. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the Bendini Cloud Application?

Bendini Cloud Application is a medical device that received FDA 510(k) clearance on 2024-08-02. The listed applicant is Nuvasive. The 510(k) number is K233706.

When did Bendini Cloud Application receive FDA 510(k) clearance?

Bendini Cloud Application received FDA 510(k) clearance on 2024-08-02, under 510(k) number K233706.

Who is the listed applicant for Bendini Cloud Application?

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

What is the FDA product code for Bendini Cloud Application?

The FDA product code for Bendini Cloud Application is OLO.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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Связанные устройства (Код: OLO)

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Официальный источник

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