FDA UDI In Commercial Distribution 🇺🇸 United States

StaXx® IB System

DI: 10840642102611 · Model: 11-1902 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
StaXx® IB System
Primary DI
10840642102611
Version / Model
11-1902
Catalog Number
11-1902
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
fa779331-cc00-425d-a852-992ef1aa02d2

Device Description

Cartridge Convex Expandable Implant 25x12x9mm

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
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 10840642102611

Customer Contacts

Phone
203-944-9494

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Width 12 Millimeter
Height 9 Millimeter