FDA UDI In Commercial Distribution 🇺🇸 United States

EVOS Lumbar Interbody System

DI: 00841193122045 · Model: CES-497 · 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
00841193122045
Version / Model
CES-497
Catalog Number
CES-497
Company Name
Cutting Edge Spine, LLC
Labeler DUNS
069472647
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
2
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
119a61a8-4870-4ca2-9dd6-bea04ddc552a

Device Description

Bayonet Box Curette, Angled

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00841193122045

Customer Contacts

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

Premarket Submissions

Submission Number Supplement Number
K150321 000

Device Sizes

Type Value Unit Text
Length 600 Millimeter

Storage Conditions

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