FDA UDI In Commercial Distribution 🇺🇸 United States

CarboClear Posterior Cervical Screw System

DI: 07290117355015 · Model: Cervical Screw · CARBOFIX ORTHOPEDICS LTD
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CarboClear Posterior Cervical Screw System
Primary DI
07290117355015
Version / Model
Cervical Screw
Catalog Number
CS5040
Company Name
CARBOFIX ORTHOPEDICS LTD
Labeler DUNS
649185170
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-19
Public Version
1
Public Version Date
2025-05-27
Public Version Status
New
Public Device Record Key
c874ffcb-61ef-4e03-91d4-1c584ae06e58

Device Description

Posterior cervical screw

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
NKG Posterior Cervical Screw System
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Package 17290117355012
Primary 07290117355015

Customer Contacts

Phone
+97299511511

Premarket Submissions

Submission Number Supplement Number
K233989 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.0 Millimeter
Length 40 Millimeter