FDA 510(k)

CarboClear® Hybrid Pedicle Screw System

N.º K: K243106 · 2024-11-05

Fecha de decisión2024-11-05

Código de productoNKB

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

CarboClear® Hybrid Pedicle Screw System 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 2024-11-05 under 510(k) number K243106. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CarboClear® Hybrid Pedicle Screw System?

CarboClear® Hybrid Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2024-11-05. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K243106.

When did CarboClear® Hybrid Pedicle Screw System receive FDA 510(k) clearance?

CarboClear® Hybrid Pedicle Screw System received FDA 510(k) clearance on 2024-11-05, under 510(k) number K243106.

Who is the listed applicant for CarboClear® Hybrid Pedicle Screw System?

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® Hybrid Pedicle Screw System?

The FDA product code for CarboClear® Hybrid Pedicle Screw System is NKB.

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Otros registros que enlistan a CarboFix Orthopedics , Ltd. como solicitante

K254045CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System K233793CarboClear® X Pedicle Screw System K240846CarboClear® 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 Cement K233989CarboClear® Posterior Cervical Screw System K233944CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments K232341CarboClear® Pedicle Screw System

Ver todos los 25 dispositivos →

Dispositivos relacionados (Código: NKB)

K252139Kentrospine Viktr-MIS® Pedicle screw systemRivarp Medical Pvt., Ltd.K262067iFuse Granite Onyx™ Implant SystemSI-BONE, Inc.K262091FRAXION Spinal Fixation SystemOrtler Global Tibbi Gerecler Anonim Sirketi K262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix Medical K262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

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