FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System

K Number: K254045 · Decision Mar 16, 2026
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
32
Review Days
89

Basic Information

Device Name
CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System
K Number
K254045
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CarboFix Orthopedics , Ltd.
Date Received
December 17, 2025
Decision Date
March 16, 2026
Product Code
NKG
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NKG Posterior Cervical Screw System

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Other Clearances by CarboFix Orthopedics , Ltd.

K Number Device Name
K243106 CarboClear® Hybrid Pedicle Screw System
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K233989 CarboClear® Posterior Cervical Screw System
K233944 CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments
K232341 CarboClear® Pedicle Screw System
K231280 CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X Fenestrated Pedicle Screw System with High V+® Bone Cement
K210716 CarboClear X Pedicle Screw System, CarboClear X Navigated Instruments
K203317 CarboClear X Pedicle Screw System
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