FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929034071 · Model: 56Z-32L-12-SP · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929034071
Version / Model
56Z-32L-12-SP
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-26
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
fd5e2c9f-58c8-4baf-968b-e22c6d94feb8

Device Description

TLIF Articulating 10°, 32Dx10Wx12H

Device Characteristics

Single Use
Yes
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
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 00889929034071

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K191408 000

Device Sizes

Type Value Unit Text
Angle 10 degree
Height 12 Millimeter
Width 10 Millimeter
Length 32 Millimeter