Aviso: Este site agrega dados públicos oficiais da FDA, ClinicalTrials.gov, PubMed e SEC EDGAR apenas para referência geral. Não constitui aconselhamento médico, diagnóstico, recomendação de tratamento ou aconselhamento de investimento.

FDA PMA

Tissue graft of 6mm and greater

Número do PMA: P020049 · 2018-09-28

RequerenteLeMaitre Vascular, Inc.
Data da decisão2018-09-28
Número PMAP020049
Código do produtoLXA
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoCV

Resumo do dispositivo

Tissue graft of 6mm and greater is the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2018-09-28. The device is classified under product code LXA. It was reviewed by the CV advisory panel.

Perguntas frequentes

What is the Tissue graft of 6mm and greater?

Tissue graft of 6mm and greater is a medical device that received FDA 510(k) clearance on 2018-09-28. The listed applicant is LeMaitre Vascular, Inc..

When did Tissue graft of 6mm and greater receive FDA 510(k) clearance?

The clearance date for Tissue graft of 6mm and greater can be found in the official FDA records.

Who is the listed applicant for Tissue graft of 6mm and greater?

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

What is the FDA product code for Tissue graft of 6mm and greater?

The FDA product code for Tissue graft of 6mm and greater is LXA.

Ensaios clínicos relacionados

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.

↑