FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929029916 · Model: 50M-1416P-13-SP · NEXXT SPINE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929029916
Version / Model
50M-1416P-13-SP
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-07
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
f4fb7b35-89d8-433c-804a-dbe37f0b7490

Device Description

Cervical Parallel 14Dx16Wx13H

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

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00889929029916

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K171140 000

Device Sizes

Type Value Unit Text
Length 14 Millimeter
Width 16 Millimeter
Height 13 Millimeter
Angle 0 degree