FDA UDI In Commercial Distribution 🇺🇸 United States

Leva® Spacer System

DI: 10840642108019 · Model: 10-7132.3 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Leva® Spacer System
Primary DI
10840642108019
Version / Model
10-7132.3
Catalog Number
10-7132.3
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
ee6b209e-596e-48f6-89c7-2f3e31472a7e

Device Description

Leva® PX Link Assembly

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
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 10840642108019

Customer Contacts

Phone
203-944-9494