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

CarboClear® Cervical Plate System

K Number: K200883 · Decision Jun 4, 2020
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
32
Review Days
63

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Basic Information

Device Name
CarboClear® Cervical Plate System
K Number
K200883
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CarboFix Orthopedics , Ltd.
Date Received
April 2, 2020
Decision Date
June 4, 2020
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

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Other Clearances by CarboFix Orthopedics , Ltd.

K Number Device Name
K254045 CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System
K243106 CarboClear® Hybrid Pedicle Screw System
K233793 CarboClear® X Pedicle Screw System
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
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
Search all 32 clearances from CarboFix Orthopedics , Ltd. →