FDA UDI In Commercial Distribution 🇺🇸 United States

Leva® Spacer System

DI: 10840642106770 · Model: 11-7224 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Leva® Spacer System
Primary DI
10840642106770
Version / Model
11-7224
Catalog Number
11-7224
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-26
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
cf6712ee-3deb-4c61-9ad5-01ab20575e9f

Device Description

Expandable Implant 22mm x 10mm x 14mm 10 Degree Lordotic

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
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 10840642106770

Customer Contacts

Phone
203-944-9494

Device Sizes

Type Value Unit Text
Height 14 Millimeter
Width 10 Millimeter
Length 22 Millimeter
Angle 10 degree