510(k) K231743

Device
F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System
Applicant
Corelink, LLC
510(k) number
K231743
Product code
MAX
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-08
Date received
2023-06-14
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
No

Applicant Contact#

Contact
Steven Mounts
Address
2072 Fenton Logistics Park St. Louis MO US 63026 63026

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code MAX#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.2026-07-17
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K250773Luna® Ti Interbody Fusion SystemSpinal Elements, Inc.2026-02-04
K253748Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemLife Spine, Inc.2026-01-23
K253266Titanium Interbody SystemSpine Innovation, LLC2026-01-08