FDA 510(k)

OMNIBotics Knee System

Номер K: K163338 · 2017-09-01

Дата решения2017-09-01

Код продуктаOLO

Консультативный комитетNE

РешениеSubstantially Equivalent

Описание устройства

OMNIBotics Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Omnllife Science, Inc.. It received FDA 510(k) clearance on 2017-09-01 under 510(k) number K163338. 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 OMNIBotics Knee System?

OMNIBotics Knee System is a medical device that received FDA 510(k) clearance on 2017-09-01. The listed applicant is Omnllife Science, Inc.. The 510(k) number is K163338.

When did OMNIBotics Knee System receive FDA 510(k) clearance?

OMNIBotics Knee System received FDA 510(k) clearance on 2017-09-01, under 510(k) number K163338.

Who is the listed applicant for OMNIBotics Knee System?

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

What is the FDA product code for OMNIBotics Knee System?

The FDA product code for OMNIBotics Knee System 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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