FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mosaic

DI: 08406061010965 · Model: 51412-411 · SPINAL ELEMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mosaic
Primary DI
08406061010965
Version / Model
51412-411
Company Name
SPINAL ELEMENTS, INC.
Labeler DUNS
610712213
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-26
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
30a7eea2-9e86-4213-8315-73e03076c3ef
Distribution End Date
2019-08-09

Device Description

14MM X 12MM X 11MM MOSAIC 4-HOLE

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
Yes
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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 08406061010965

Customer Contacts