FDA UDI In Commercial Distribution 🇺🇸 United States

CarboClear Lumbar Cage System

DI: 07290110208752 · Model: Cubic Lordotic Cage · CARBOFIX ORTHOPEDICS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CarboClear Lumbar Cage System
Primary DI
07290110208752
Version / Model
Cubic Lordotic Cage
Catalog Number
CCLC231210
Company Name
CARBOFIX ORTHOPEDICS LTD
Labeler DUNS
649185170
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-20
Public Version
1
Public Version Date
2021-01-28
Public Version Status
New
Public Device Record Key
af1a03d6-0fb2-42b9-9a8e-320101af98bf

Device Description

A lumbar intervertebral body fusion device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary 07290110208752

Customer Contacts

Phone
+97299511511

Premarket Submissions

Submission Number Supplement Number
K203683 000

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Length 23 Millimeter
Height 12 Millimeter
Angle 10 degree