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FDA PMA

Stimulator, spinal-cord, totally implanted for pain relief

Número do PMA: P010032 · 2026-09-23

RequerenteABBOTT MEDICAL
Data da decisão2026-09-23
Número PMAP010032
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 ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-09-23. 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 2026-09-23. The listed applicant is ABBOTT MEDICAL.

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 ABBOTT MEDICAL 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.

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Fonte oficial

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