QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)
K-Number: K260362 · 2026-07-24
Device Summary
Frequently Asked Questions
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)?
The FDA product code for QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration) is NKB.
Related Devices (Code: NKB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.