FDA UDI In Commercial Distribution 🇺🇸 United States

COLONIAL

DI: 00849044029314 · Model: 365.307 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COLONIAL
Primary DI
00849044029314
Version / Model
365.307
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-06
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
8096b5a3-6c28-4513-91ad-877d89338f57

Device Description

Colonial ACDF Spacer, Large, Parallel, 7mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00849044029314

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072991 000

Device Sizes

Type Value Unit Text
Width 14 Millimeter
Height 7 Millimeter
Depth 12 Millimeter