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FDA PMA

Prosthesis, spinous process spacer/plate

Número do PMA: P110008 · 2026-05-22

RequerenteCompanion Spine France
Data da decisão2026-05-22
Número PMAP110008
Código do produtoNQO
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoOR

Resumo do dispositivo

Prosthesis, spinous process spacer/plate is the device name listed in this FDA 510(k) record. The listed applicant is Companion Spine France. It received FDA 510(k) clearance on 2026-05-22. The device is classified under product code NQO. It was reviewed by the OR advisory panel. Product code NQO falls under the category of General Hospital, which covers general-purpose hospital equipment and supplies. Devices in this category are subject to specific FDA regulatory requirements.

Perguntas frequentes

What is the Prosthesis, spinous process spacer/plate?

Prosthesis, spinous process spacer/plate is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Companion Spine France.

When did Prosthesis, spinous process spacer/plate receive FDA 510(k) clearance?

The clearance date for Prosthesis, spinous process spacer/plate can be found in the official FDA records.

Who is the listed applicant for Prosthesis, spinous process spacer/plate?

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

What is the FDA product code for Prosthesis, spinous process spacer/plate?

The FDA product code for Prosthesis, spinous process spacer/plate is NQO. This falls under the General Hospital category.

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Fonte oficial

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