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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 the device name listed in this FDA 510(k) record. The listed applicant is CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2024-01-10 under 510(k) 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. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K233944.

When did CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments receive FDA 510(k) clearance?

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

Who is the listed applicant for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?

The FDA 510(k) record lists CarboFix Orthopedics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing CarboFix Orthopedics , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254045CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw SystemK243106CarboClear® Hybrid Pedicle Screw SystemK233793CarboClear® X Pedicle Screw SystemK240846CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments; CarboClear® Hybrid Fenestrated Pedicle Screw System and High V+® Bone Cement; CarboClear® X Fenestrated Pedicle Screw System and High V+® Bone CementK233989CarboClear® Posterior Cervical Screw SystemK232341CarboClear® Pedicle Screw System

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Related Devices (Code: NKB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.K253943Tiger 2 SystemZavation Medical Products, LLCK261284Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemAlphatec Spine, Inc.K253802KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK253045“Socko” Vimax Spinal Fixation SystemSocko Medical Co., Ltd.K251251ChanPin Pedicle Screw Spinal SystemChanpin Medtak Co., Ltd.

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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