FDA UDI In Commercial Distribution 🇺🇸 United States

LLIF Interbody System

DI: 00195860007679 · Model: LL00185508 · Evolution Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LLIF Interbody System
Primary DI
00195860007679
Version / Model
LL00185508
Catalog Number
LL00185508
Company Name
Evolution Spine LLC
Labeler DUNS
116940934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-12
Public Version
1
Public Version Date
2021-06-21
Public Version Status
New
Public Device Record Key
47d0d495-8509-4ec4-8deb-bb133a0a8af7

Device Description

18x55x8mm LLIF Cage 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
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00195860007679

Customer Contacts

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Depth 55 Millimeter
Device Size Text, specify Parallel
Width 18 Millimeter