FDA UDI In Commercial Distribution 🇺🇸 United States

Keystone ALIF System

DI: 00195860006894 · Model: DP-002 · Evolution Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Keystone ALIF System
Primary DI
00195860006894
Version / Model
DP-002
Catalog Number
DP-002
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
b51490c5-4053-485c-b41d-74af3db92e34

Device Description

Six-8 Distractor

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
44378 Bone distraction forceps

Identifiers

Type ID
Primary 00195860006894

Customer Contacts