FDA PMA

Prosthesis, spinous process spacer/plate

Номер PMA: P110008 · 2026-05-22

ЗаявительCompanion Spine France

Дата решения2026-05-22

Номер PMAP110008

Код продуктаNQO

Класс устройстваКласс 3

Медицинская специализацияU

Консультативный комитетOR

Описание устройства

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.

Часто задаваемые вопросы

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.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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Официальный источник

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