FDA 510(k)

QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)

Número K: K260362 · 2026-07-24

Data da decisão2026-07-24

Código do produtoNKB

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration) is the device name listed in this FDA 510(k) record. The listed applicant is MANTIZ Co., Ltd.. It received FDA 510(k) clearance on 2026-07-24 under 510(k) number K260362. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)?

QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration) is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is MANTIZ Co., Ltd.. The 510(k) number is K260362.

When did QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration) receive FDA 510(k) clearance?

QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration) received FDA 510(k) clearance on 2026-07-24, under 510(k) number K260362.

Who is the listed applicant for QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)?

The FDA 510(k) record lists MANTIZ Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)?

O código de produto da FDA para o sistema vertebral QUATTRO (Configuração Aberta); sistema vertebral QUATTRO-GADGET (Configuração MIS) é NKB.

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