FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929022658 · Model: C50-01-01 · NEXXT SPINE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929022658
Version / Model
C50-01-01
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-22
Public Version
7
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
52ee35f4-cd9e-48a1-a584-4295d92cc058

Device Description

Cervical Interbody Tray

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical
MQP Spinal Vertebral Body Replacement Device

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00889929022658

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K171140 000