FDA UDI In Commercial Distribution 🇺🇸 United States

EVOS Lumbar Interbody System

DI: 00841193109237 · Model: 4113-010 · Cutting Edge Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVOS Lumbar Interbody System
Primary DI
00841193109237
Version / Model
4113-010
Catalog Number
4113-010
Company Name
Cutting Edge Spine, LLC
Labeler DUNS
069472647
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
78f49059-b335-47bc-815e-754406ed6de0

Device Description

HA PEEK EVOS Straight, ,10mmx8mmx 26mm , FLAT 5 ° , Wide Nose

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
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
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 00841193109237

Customer Contacts

Phone
+1(704)243-0892 ext. 10

Premarket Submissions

Submission Number Supplement Number
K150321 000

Device Sizes

Type Value Unit Text
Length 26 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature