Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments

K-Number: K233944 · 2024-01-10

ApplicantCarboFix Orthopedics , Ltd.
Decision Date2024-01-10
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments is a medical device manufactured by CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2024-01-10 under approval number K233944. 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 CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments is a medical device that received FDA 510(k) clearance on 2024-01-10. It is manufactured by CarboFix Orthopedics , Ltd.. The 510(k) number is K233944.

When was CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments approved by the FDA?

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments received FDA 510(k) clearance on 2024-01-10, under approval number K233944.

What company makes CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments is manufactured by CarboFix Orthopedics , Ltd..

What is the FDA product code for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?

The FDA product code for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments is NKB.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT07596550 Comparative Study of Augmented Reality and Virtual Reality in Music Therapy Interventions for Individuals With Cerebral Palsy NOT_YET_RECRUITING NCT05762055 Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology ENROLLING_BY_INVITATION NCT06411054 The Efficacy of Acu-TENS as an Adjunct Analgesic During USG-MVA RECRUITING NCT07578142 AcceXible Speech-Based Screening for Depression and Anxiety in University Students (UAQ, Mexico) NOT_YET_RECRUITING NCT07578155 Validation of Accexible Screening and Self-Administered Activities for Emotional Well-Being in a University Hospital (UaDEC) COMPLETED

Related PubMed Literature

PMID: 41619565 Integration of materiovigilance in Unani medicine: A step towards patient safety. Journal of Ayurveda and integrative medicine (2026) 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 CarboFix Orthopedics , Ltd.

K160002Piccolo Composite(R) Distal Volar Radius Plate System K153536Piccolo Composite® Nailing System K173652Piccolo Composite Nailing System K170401Piccolo Composite® Plate System K182015Piccolo Composite® Plate System K182377CarboClear® Pedicle Screw System

View all 25 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.

↑