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

CarboClear Lumbar Cage System

K Number: K193378 · Decision Mar 2, 2020
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
17
Review Days
88

Basic Information

Device Name
CarboClear Lumbar Cage System
K Number
K193378
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CarboFix Orthopedics Ltd.
Date Received
December 5, 2019
Decision Date
March 2, 2020
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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Other Clearances by CarboFix Orthopedics Ltd.

K Number Device Name
K233793 CarboClear® X Pedicle Screw System
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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
K192214 CarboClear VBR System
K190526 High V+ Bone Cement, CarboClear® Fenestrated Pedicle Screws
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