FDA UDI In Commercial Distribution 🇺🇸 United States

Vusion TS

DI: 00822409033751 · Model: 551-1113A · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vusion TS
Primary DI
00822409033751
Version / Model
551-1113A
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
2020-02-24
Public Version Status
Update
Public Device Record Key
2ade7bb2-0df0-415e-b1ab-0d1108135915

Device Description

13 mm 6 Degree Lordotic

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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00822409033751

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K062666 000

Device Sizes

Type Value Unit Text
Angle 6 degree
Height 13 Millimeter