FDA UDI In Commercial Distribution 🇺🇸 United States

C-Box®

DI: M71112507130 · Model: 1250713 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
C-Box®
Primary DI
M71112507130
Version / Model
1250713
Catalog Number
1250713
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-01-22
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
47c7a4ad-eaf4-4266-8fc8-8e5e40660ec6

Device Description

PEEK, Ta

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
Yes
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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M71112507130

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K132991 000

Device Sizes

Type Value Unit Text
Width 13.5 Millimeter
Height 7 Millimeter
Length 12.5 Millimeter