FDA UDI In Commercial Distribution 🇺🇸 United States

LLIF Interbody System

DI: 00195860007976 · Model: LLI02 · Evolution Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LLIF Interbody System
Primary DI
00195860007976
Version / Model
LLI02
Catalog Number
LLI02
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
3574e797-dd44-4961-a1b4-8a2ac2177f67

Device Description

Lateral Slap Hammer

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
Yes
PM Exempt
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47814 Orthopaedic implantation hammering attachment

Identifiers

Type ID
Primary 00195860007976

Customer Contacts