FDA UDI Not in Commercial Distribution 🇺🇸 United States

ZEUS-C

DI: 00840916119911 · Model: 1001108LL-STR · SPINAL ELEMENTS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZEUS-C
Primary DI
00840916119911
Version / Model
1001108LL-STR
Company Name
SPINAL ELEMENTS
Labeler DUNS
004022104
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-17
Public Version
4
Public Version Date
2021-03-31
Public Version Status
Update
Public Device Record Key
98564a0b-f33f-46f2-94d7-a0035d6168a7
Distribution End Date
2021-03-30

Device Description

Zeus Cervical 17x14x8 Sterile

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
Yes
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 00840916119911