FDA.report

510(k) K260549

Device
ZSFab Cervical Interbody System and ZSFab Lumbar Interbody System
Applicant
Zsfab, Inc.
510(k) number
K260549
Product code
ODP
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-24
Date received
2026-02-18
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Yuanqiao Wu
Address
96 Clematis Ave. Suite 2f Waltham MA US 02453 02453

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

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K253260ORIO-3D Cage SystemSpineCraft2026-04-16
K260340HC BIOLOGICS OSTEOPOINT PEEK CAGES, HC BIOLOGICS OSTEOPOINT CERVICAL PEEK CAGES, HC BIOLOGICS OSTEOPOINT LUMBAR PEEK CAGESHC Biologics, LLC2026-04-13
K242303MOD-COrthomod, LLC2026-04-01
K252240Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage SystemSpectrum Spine2026-03-30
K252432Flex-Z™ Cervical CageSpinepoint, LLC2026-03-25
K254105Hive™ Standalone Cervical System and Hive™ C Interbody SystemNanoHive Medical, LLC2026-02-13
K252205Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF SystemCuriteva, Inc.2026-01-16
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