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

Stimulator, spinal-cord, totally implanted for pain relief

Número do PMA: P130028 · 2020-05-05

RequerenteNuvectra Corporation
Data da decisão2020-05-05
Número PMAP130028
Código do produtoLGW
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoNE

Resumo do dispositivo

Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Nuvectra Corporation. It received FDA 510(k) clearance on 2020-05-05. The device is classified under product code LGW. It was reviewed by the NE advisory panel.

Perguntas frequentes

What is the Stimulator, spinal-cord, totally implanted for pain relief?

Stimulator, spinal-cord, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Nuvectra Corporation.

When did Stimulator, spinal-cord, totally implanted for pain relief receive FDA 510(k) clearance?

The clearance date for Stimulator, spinal-cord, totally implanted for pain relief can be found in the official FDA records.

Who is the listed applicant for Stimulator, spinal-cord, totally implanted for pain relief?

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

What is the FDA product code for Stimulator, spinal-cord, totally implanted for pain relief?

The FDA product code for Stimulator, spinal-cord, totally implanted for pain relief is LGW.

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.

↑