FDA UDI In Commercial Distribution 🇺🇸 United States

Vusion OS

DI: 00822409020355 · Model: 551-6308A · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vusion OS
Primary DI
00822409020355
Version / Model
551-6308A
Catalog Number
551-6308A
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-15
Public Version
4
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
4d43eb20-5c2d-49a7-8bcc-b750d16ea763

Device Description

Vusion OS 9mm x 30mm x 8mm x Parallel

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
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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00822409020355

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111965 000

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Length 30 Millimeter
Width 9 Millimeter