510(k) K260506

Device
Ventana® P/T Lumbar Interbody System
Applicant
Spinal Elements, Inc.
510(k) number
K260506
Product code
MAX
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-15
Date received
2026-02-17
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Lumbar
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
Sartaj Kaur-Hurrle
Address
3115 Melrose Dr. Suite 200 Carlsbad CA US 92010 92010

FDA Registration Numbers

Source Documents

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

Other 510(k) Records For Product Code MAX

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K252610ZSFab Lumbar Interbody SystemZsfab, Inc.2025-11-25
K252351UniSpace® TPLIF CageCg Medtech Co., Ltd.2025-10-28
K253377Expandable Titanium PLIF/TLIF SystemSpectrum Spine, Inc.2025-10-24
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K251444Endoskeleton™ Interbody SystemsMedtronic Sofamor Danek USA, Inc.2025-09-04
K251969Atlas Spine Project X Expandable Posterior Lumbar Interbody SystemAtlas Spine, Inc.2025-08-15