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FDA 510(k)

INERTIA CONNEXX Modular Pedicle Screw System

K-Number: K221905 · 2022-07-28

ApplicantNexxt Spine, LLC
Decision Date2022-07-28
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INERTIA CONNEXX Modular Pedicle Screw System is a medical device manufactured by Nexxt Spine, LLC. It received FDA 510(k) clearance on 2022-07-28 under approval number K221905. 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 INERTIA CONNEXX Modular Pedicle Screw System?

INERTIA CONNEXX Modular Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2022-07-28. It is manufactured by Nexxt Spine, LLC. The 510(k) number is K221905.

When was INERTIA CONNEXX Modular Pedicle Screw System approved by the FDA?

INERTIA CONNEXX Modular Pedicle Screw System received FDA 510(k) clearance on 2022-07-28, under approval number K221905.

What company makes INERTIA CONNEXX Modular Pedicle Screw System?

INERTIA CONNEXX Modular Pedicle Screw System is manufactured by Nexxt Spine, LLC.

What is the FDA product code for INERTIA CONNEXX Modular Pedicle Screw System?

The FDA product code for INERTIA CONNEXX Modular Pedicle Screw System is NKB.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT04798768 Effectiveness of the EMPOWER™ Modular Pacing System and EMBLEM™ Subcutaneous ICD to Communicate Antitachycardia Pacing ACTIVE_NOT_RECRUITING NCT05762055 Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology ENROLLING_BY_INVITATION NCT04358601 All-poly Versus Metal-backed ACTIVE_NOT_RECRUITING NCT05565131 Performance Measurement and Safety Evaluation of the PYTHEAS® ODYSSEE Angular Assistance System for Intra-pedicular Screw Placement in Adult Spine Surgery COMPLETED NCT06720948 The ION Facet Screw System Ambispective Evaluation ENROLLING_BY_INVITATION

Related PubMed Literature

PMID: 41487949 Verification, validation, and uncertainty quantification of finite element analysis results for pedicle screw assemblies under ASTM F1717 flexion and extension testing. Frontiers in bioengineering and biotechnology (2025)

Other Devices by Nexxt Spine, LLC

K153453Inertia Pedicle Screw and Deformity Correxxion System K171140Matrixx System K182508Saxxony™ Posterior Cervical Thoracic System K191408Nexxt Matrixx System K190546NEXXT MATRIXX Stand Alone Cervical System K202230NEXXT MATRIXX Stand Alone ALIF System

View all 15 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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