FDA UDI In Commercial Distribution 🇺🇸 United States

C-THRU™ Anterior Spinal System

DI: 00880304908239 · Model: 55001910 · BIOMET SPINE LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
C-THRU™ Anterior Spinal System
Primary DI
00880304908239
Version / Model
55001910
Catalog Number
55001910
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-23
Public Version
2
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
17ae7c69-6a7a-4c5b-9403-abc524bf706a

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQP Spinal vertebral body replacement device
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00880304908239

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Lordotic 11 x 11 x 10 mm PEEK Spacer with X-Ray Markers