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

CarboClear VBR System

K Number: K192214 · Decision Oct 11, 2019
Classifications
1
FEI Numbers
215
Registration Numbers
215
Same Product Code
275
Applicant Total
17
Review Days
57

Basic Information

Device Name
CarboClear VBR System
K Number
K192214
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
August 15, 2019
Decision Date
October 11, 2019
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

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Other Clearances by CarboFix Orthopedics Ltd.

K Number Device Name
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
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
K190526 High V+ Bone Cement, CarboClear® Fenestrated Pedicle Screws
Search all 17 clearances from CarboFix Orthopedics Ltd. →