FDA UDI In Commercial Distribution 🇺🇸 United States

nva

DI: 90814008024585 · Model: ALE-1220-S · NVISION BIOMEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
nva
Primary DI
90814008024585
Version / Model
ALE-1220-S
Company Name
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Labeler DUNS
047486041
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-15
Public Version
6
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
37272547-8d8b-444c-92cf-efde48dd77dd

Device Description

ALIF Encoded 25x34 20mm 12 Degree

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
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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 90814008024585

Customer Contacts

Phone
210-545-3713

Premarket Submissions

Submission Number Supplement Number
K142594 000

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Width 34 Millimeter
Height 20 Millimeter
Angle 12 degree
Device Size Text, specify 25x34 20mm 12 degree