FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929052709 · Model: 50A-1618-09-SP · NEXXT SPINE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929052709
Version / Model
50A-1618-09-SP
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-17
Public Version
1
Public Version Date
2023-07-25
Public Version Status
New
Public Device Record Key
700c4d46-b671-4cb7-92bf-0a2db37f661c

Device Description

Convexx Cervical 16Dx18Wx9H

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
ODP Intervertebral Fusion Device With Bone Graft, Cervical
MQP Spinal Vertebral Body Replacement Device

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00889929052709

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K171140 000

Device Sizes

Type Value Unit Text
Width 18 Millimeter
Depth 16 Millimeter
Angle 6 degree
Height 9 Millimeter