FDA 510(k)

Montage Settable Bone Putty

Número K: K242050 · 2024-07-29

Data da decisão2024-07-29

Código do produtoMQV

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Montage Settable Bone Putty is the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2024-07-29 under 510(k) number K242050. 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 Montage Settable Bone Putty?

Montage Settable Bone Putty is a medical device that received FDA 510(k) clearance on 2024-07-29. The listed applicant is Orthocon, Inc.. The 510(k) number is K242050.

When did Montage Settable Bone Putty receive FDA 510(k) clearance?

Montage Settable Bone Putty received FDA 510(k) clearance on 2024-07-29, under 510(k) number K242050.

Who is the listed applicant for Montage Settable Bone Putty?

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

What is the FDA product code for Montage Settable Bone Putty?

The FDA product code for Montage Settable Bone Putty is MQV.

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Fonte oficial

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