FDA UDI In Commercial Distribution 🇺🇸 United States

TiNano

DI: B5211050200060 · Model: DISCOVERY · AURORA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TiNano
Primary DI
B5211050200060
Version / Model
DISCOVERY
Catalog Number
105-020-006
Company Name
AURORA SPINE, INC.
Labeler DUNS
079119091
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-01
Public Version
2
Public Version Date
2019-03-15
Public Version Status
Update
Public Device Record Key
dbccb921-fde4-49ca-8877-7a2ce6abb50c

Device Description

DISCOVERY Cervical Interbody Fusion System, 15mm x 18mm x 0 degrees x 6mm

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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary B5211050200060

Customer Contacts

Phone
760.424.2004

Premarket Submissions

Submission Number Supplement Number
K111484 000

Device Sizes

Type Value Unit Text
Height 6 Millimeter
Angle 0 degree
Width 18 Millimeter
Length 15 Millimeter