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FDA PMA

Dispositivo de reparo da válvula tricúspide, fornecido percutaneamente

Número do PMA: P230007 · 2026-06-25

RequerenteABBOTT MEDICAL
Data da decisão2026-06-25
Número PMAP230007
Código do produtoNPS
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoCV

Resumo do dispositivo

Tricuspid valve repair device, percutaneously delivered is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-06-25. The device is classified under product code NPS. It was reviewed by the CV advisory panel.

Perguntas frequentes

What is the Tricuspid valve repair device, percutaneously delivered?

Tricuspid valve repair device, percutaneously delivered is a medical device that received FDA 510(k) clearance on 2026-06-25. The listed applicant is ABBOTT MEDICAL.

When did Tricuspid valve repair device, percutaneously delivered receive FDA 510(k) clearance?

The clearance date for Tricuspid valve repair device, percutaneously delivered can be found in the official FDA records.

Who is the listed applicant for Tricuspid valve repair device, percutaneously delivered?

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

What is the FDA product code for Tricuspid valve repair device, percutaneously delivered?

The FDA product code for Tricuspid valve repair device, percutaneously delivered is NPS.

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Fonte oficial

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