FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929055779 · Model: I92-12-03 · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929055779
Version / Model
I92-12-03
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-11
Public Version
1
Public Version Date
2025-03-19
Public Version Status
New
Public Device Record Key
51f059c9-e909-4c79-8d71-f790116afd13

Device Description

Dual Sided Rasp, 6mm, Angled

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00889929055779

Customer Contacts

Phone
317-436-7801

Device Sizes

Type Value Unit Text
Device Size Text, specify 6
Angle 15 degree