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

CarboClear® Posterior Cervical Screw System

K Number: K233989 · Decision Mar 27, 2024
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
112
Applicant Total
17
Review Days
100

Basic Information

Device Name
CarboClear® Posterior Cervical Screw System
K Number
K233989
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 18, 2023
Decision Date
March 27, 2024
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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K Number Device Name
K233793 CarboClear® X Pedicle Screw System
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K210716 CarboClear X Pedicle Screw System, CarboClear X Navigated Instruments
K203317 CarboClear X Pedicle Screw System
K201926 CarboClear® Pedicle Screw System, CarboClear® II Pedicle Screw System
K201251 CarboClear Navigated Instruments
K200519 CarboClear® II Pedicle Screw System
K193378 CarboClear Lumbar Cage System
K192214 CarboClear VBR System
K190526 High V+ Bone Cement, CarboClear® Fenestrated Pedicle Screws
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