510(k) K260840

Device
BluEX Cervical Expandable Cage System
Applicant
L&K BIOMED Co., Ltd.
510(k) number
K260840
Product code
ODP
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-16
Date received
2026-03-16
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Kihyang Kim
Address
#101, 201, 202 16-25, Dongbaekjungang-Ro 16 Beon-Gil Giheung-Gu, Yongin-Si KR 17015 17015

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code ODP

510(k)DeviceApplicantDecision date
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K252432Flex-Z™ Cervical CageSpinepoint, LLC2026-03-25
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K254061Curiteva Porous PEEK Cervical Interbody Fusion SystemCuriteva, Inc.2026-01-15
K252219Cervical Interbody and VBR Fusion SystemSync Surgical2026-01-14
K252711Advantage-C™ Ti3D Cervical Interbody Fusion DeviceIntelivation Technologies2026-01-08
K252894aprevo® cervical interbody systemCarlsmed, Inc.2026-01-06
K252781MSFX MIKRON PEEK CAGESMikron Makina Sanayi VE Tic. Ltd. Sti.2025-12-19
K250764SpineLinc Anterior Cervical Implant SystemLincotek Medical2025-12-05