FDA 510(k)

MagnetOs Putty

Número K: K181958 · 2018-12-06

Data da decisão2018-12-06

Código do produtoMQV

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

MagnetOs Putty is the device name listed in this FDA 510(k) record. The listed applicant is Kuros Biosciences B.V. It received FDA 510(k) clearance on 2018-12-06 under 510(k) number K181958. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MagnetOs Putty?

MagnetOs Putty is a medical device that received FDA 510(k) clearance on 2018-12-06. The listed applicant is Kuros Biosciences B.V. The 510(k) number is K181958.

When did MagnetOs Putty receive FDA 510(k) clearance?

MagnetOs Putty received FDA 510(k) clearance on 2018-12-06, under 510(k) number K181958.

Who is the listed applicant for MagnetOs Putty?

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

What is the FDA product code for MagnetOs Putty?

The FDA product code for MagnetOs Putty is MQV.

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K243474MagnetOs MIS K240442MagnetOs Putty K232347MagnetOs Granules K230736MagnetOs Putty K233607MagnetOs Easypack Putty K233245MagnetOs Flex Matrix

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Fonte oficial

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