FDA 510(k)

BEE HA Cage

Número K: K203444 · 2021-03-18

Data da decisão2021-03-18

Código do produtoODP

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

BEE HA Cage is the device name listed in this FDA 510(k) record. The listed applicant is NGMedical GmbH. It received FDA 510(k) clearance on 2021-03-18 under 510(k) number K203444. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the BEE HA Cage?

BEE HA Cage is a medical device that received FDA 510(k) clearance on 2021-03-18. The listed applicant is NGMedical GmbH. The 510(k) number is K203444.

When did BEE HA Cage receive FDA 510(k) clearance?

BEE HA Cage received FDA 510(k) clearance on 2021-03-18, under 510(k) number K203444.

Who is the listed applicant for BEE HA Cage?

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

What is the FDA product code for BEE HA Cage?

The FDA product code for BEE HA Cage is ODP.

Outros registros que listam NGMedical GmbH como candidato(a)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

K261067BEE PLIF Cage K250560BEE HA K231371BEE Cervical Cage K212050NGM WAVE PLIF Cage K211413BEE PLIF Cage K200429BEE Cages

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Fonte oficial

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