FDA UDI In Commercial Distribution 🇺🇸 United States

C-THRU™ Anterior Spinal System

DI: 00880304911697 · Model: 14-531201 · 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
00880304911697
Version / Model
14-531201
Catalog Number
14-531201
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-12
Public Version
2
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
b0f0a029-796a-499f-87de-4ea4f11b354a

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

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00880304911697

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Convex 18 x 16 x 11 mm PEEK Spacer with X-Ray Markers