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FDA 510(k)

Cogent Lateral Interbody System

K-Number: K151406 · 2016-02-25

ApplicantCogent Spine, LLC
Decision Date2016-02-25
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cogent Lateral Interbody System is a medical device manufactured by Cogent Spine, LLC. It received FDA 510(k) clearance on 2016-02-25 under approval number K151406. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cogent Lateral Interbody System?

Cogent Lateral Interbody System is a medical device that received FDA 510(k) clearance on 2016-02-25. It is manufactured by Cogent Spine, LLC. The 510(k) number is K151406.

When was Cogent Lateral Interbody System approved by the FDA?

Cogent Lateral Interbody System received FDA 510(k) clearance on 2016-02-25, under approval number K151406.

What company makes Cogent Lateral Interbody System?

Cogent Lateral Interbody System is manufactured by Cogent Spine, LLC.

What is the FDA product code for Cogent Lateral Interbody System?

The FDA product code for Cogent Lateral Interbody System is MAX.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT07616050 Evaluation of the Impact of Virtual Park on Training Motivation in Adult Patients NOT_YET_RECRUITING NCT05762055 Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology ENROLLING_BY_INVITATION NCT07571486 Therapeutic Approach of Repeated Transient Blood-brain Barrier Opening in Amyotrophic Lateral Sclerosis. NOT_YET_RECRUITING NCT06696365 iTBS for Alcohol Use Disorder TERMINATED NCT06638138 Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction of the Anterior Talofibular Ligament (ATFL) to Treat Lateral Ankle Instability COMPLETED

Related Devices (Code: MAX)

K163180Hubble IIOrbbo Surgical, LLC K162446FORZA Spacer System, PILLAR PEEK Spacer System, PILLAR SA PEEK Spacer System, SKYHAWK Lateral Interbody Fusion SystemOrthofix, Inc. K162327COUGAR® LS Lateral Cage System and COUGAR® SystemMedos International SARL K162103Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Interbody Fusion System (Harrier™), Choice Spine Vertebral Body Replacement System (Hawkeye™)Choicespine, LP K162431Luna 3D Interbody Fusion SystemBenvenue Medical, Inc. K160959Xsert Lumbar Expandable Interbody SystemX-Spine Systems, Inc.

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.

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