CarboClear® Pedicle Screw System

Thoracolumbosacral Pedicle Screw System

CarboFix Orthopedics Ltd.

The following data is part of a premarket notification filed by Carbofix Orthopedics Ltd. with the FDA for Carboclear® Pedicle Screw System.

Pre-market Notification Details

Device IDK173487
510k NumberK173487
Device Name:CarboClear® Pedicle Screw System
ClassificationThoracolumbosacral Pedicle Screw System
Applicant CarboFix Orthopedics Ltd. 11 Ha’hoshlim St. Herzeliya,  IL 4672411
ContactHila Wachsler-avrahami
CorrespondentHila Wachsler-avrahami
CarboFix Orthopedics Ltd. 11 Ha’hoshlim St. Herzeliya,  IL 4672411
Product CodeNKB  
CFR Regulation Number888.3070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-11-13
Decision Date2018-07-18
Summary:summary

NIH GUDID Devices

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Trademark Results [CarboClear]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CARBOCLEAR
CARBOCLEAR
86654176 5283412 Live/Registered
CarboFix In Orthopedics LLC
2015-06-07

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