FDA UDI Not in Commercial Distribution 🇺🇸 United States

ECHO TiNano PLIF

DI: B521108824080807 · Model: 108024080807 · AURORA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ECHO TiNano PLIF
Primary DI
B521108824080807
Version / Model
108024080807
Catalog Number
108824080807
Company Name
AURORA SPINE, INC.
Labeler DUNS
079119091
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-01
Public Version
5
Public Version Date
2019-02-04
Public Version Status
Update
Public Device Record Key
e848a7cb-732a-43e2-a0a3-63b8b48c55ae
Distribution End Date
2019-02-01

Device Description

ECHO TiNano PLIF 24mm X 8mm X 8 X 7mm

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary B521108824080807

Customer Contacts

Phone
999-999-9999

Premarket Submissions

Submission Number Supplement Number
K133967 000

Device Sizes

Type Value Unit Text
Height 7 Millimeter
Angle 8 degree
Width 8 Millimeter
Length 24 Millimeter