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FDA 510(k)

Reliance Spinal Screw System

K-Number: K210874 · 2021-05-13

ApplicantReliance Medical Systems, LLC
Decision Date2021-05-13
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Reliance Spinal Screw System is a medical device manufactured by Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2021-05-13 under approval number K210874. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reliance Spinal Screw System?

Reliance Spinal Screw System is a medical device that received FDA 510(k) clearance on 2021-05-13. It is manufactured by Reliance Medical Systems, LLC. The 510(k) number is K210874.

When was Reliance Spinal Screw System approved by the FDA?

Reliance Spinal Screw System received FDA 510(k) clearance on 2021-05-13, under approval number K210874.

What company makes Reliance Spinal Screw System?

Reliance Spinal Screw System is manufactured by Reliance Medical Systems, LLC.

What is the FDA product code for Reliance Spinal Screw System?

The FDA product code for Reliance Spinal Screw System is NKB.

Related Clinical Trials

NCT06998134 Toward Ubiquitous Lower Limb Exoskeleton Use in Children and Young Adults RECRUITING NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT03053791 Deep Brain Stimulation in Patients With Incomplete Spinal Cord Injury for Improvement of Gait RECRUITING NCT07616050 Evaluation of the Impact of Virtual Park on Training Motivation in Adult Patients NOT_YET_RECRUITING NCT05508360 "Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nulcectomy" (LOPAIN2) RECRUITING NCT06087445 A User-friendly, Non-invasive Neuro-orthosis That Restores Volitionally Controlled Grasp Functions for SCI Survivors With Tetraplegia COMPLETED

Related PubMed Literature

PMID: 41612341 Brain-computer interface commercialization. Journal of neuroengineering and rehabilitation (2026) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by Reliance Medical Systems, LLC

K162066Reliance Spinal Screw System K160463Reliance Lumbar IBF System K173102Reliance Cervical IBF System K172489Reliance Cervical IBF System K173283Reliance Lumbar IBF System K183049Reliance Lumbar IBF System

View all 8 devices →

Related Devices (Code: NKB)

K163301CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc. K162134ENNOVATE Spinal SystemAesculap Implant Systems, LLC K162912VIPER PRIME™ additions to the VIPER® SystemMedos International SARL K162160Preference Elite Pedicle Screw SystemAmedica Corporation K162232MOSS 100 Pedicle Screw SystemBiedermann Motech GmbH & Co. KG K162379CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, 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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