FDA UDI In Commercial Distribution 🇺🇸 United States

Aurora Spine

DI: B521108322101080 · Model: ECHO · AURORA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aurora Spine
Primary DI
B521108322101080
Version / Model
ECHO
Catalog Number
108-32210-108
Company Name
AURORA SPINE, INC.
Labeler DUNS
079119091
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-30
Public Version
1
Public Version Date
2019-05-08
Public Version Status
New
Public Device Record Key
b81ba434-7453-4ac1-8ed5-5d07f29dc78e

Device Description

ECHO, TRIAL-L, 22mm, 10mm, 8mm

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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 B521108322101080

Customer Contacts

Phone
760.424.2004

Premarket Submissions

Submission Number Supplement Number
K133967 000

Device Sizes

Type Value Unit Text
Angle 4 degree
Height 8 Millimeter
Width 10 Millimeter
Length 22 Millimeter