FDA PMA

Filler, bone void, synthetic peptide

Número do PMA: P240001 · 2026-09-16

RequerenteCerapedics, Inc.

Data da decisão2026-09-16

Número PMAP240001

Código do produtoNOX

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoOR

Resumo do dispositivo

Filler, bone void, synthetic peptide is the device name listed in this FDA 510(k) record. The listed applicant is Cerapedics, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code NOX. It was reviewed by the OR advisory panel.

Perguntas frequentes

What is the Filler, bone void, synthetic peptide?

Filler, bone void, synthetic peptide is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Cerapedics, Inc..

When did Filler, bone void, synthetic peptide receive FDA 510(k) clearance?

The clearance date for Filler, bone void, synthetic peptide can be found in the official FDA records.

Who is the listed applicant for Filler, bone void, synthetic peptide?

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

What is the FDA product code for Filler, bone void, synthetic peptide?

The FDA product code for Filler, bone void, synthetic peptide is NOX.

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Fonte oficial

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