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

CarboClear® X Pedicle Screw System

K Number: K233793 · Decision Aug 1, 2024
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
17
Review Days
247

Basic Information

Device Name
CarboClear® X Pedicle Screw System
K Number
K233793
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CarboFix Orthopedics Ltd.
Date Received
November 28, 2023
Decision Date
August 1, 2024
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKB), ordered by most recent decision date.

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Other Clearances by CarboFix Orthopedics Ltd.

K Number Device Name
K240846 CarboClear® 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
K233989 CarboClear® Posterior Cervical Screw System
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
Search all 17 clearances from CarboFix Orthopedics Ltd. →