FDA UDI In Commercial Distribution 🇺🇸 United States

VuMesh™

DI: 10889981036409 · Model: 15-10-1440 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VuMesh™
Primary DI
10889981036409
Version / Model
15-10-1440
Catalog Number
15-10-1440
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e8cb5d63-7bef-4f48-9751-4fd2e09fb260

Device Description

14mm Sq Cage X 40mm Long

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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
57806 Vertebral body prosthesis, non-sterile

Identifiers

Type ID
Primary 10889981036409

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070381 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 14mm x 40mm