FDA UDI In Commercial Distribution 🇺🇸 United States

Matrixx System

DI: 00889929027639 · Model: 51M-1618-10-SP · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Matrixx System
Primary DI
00889929027639
Version / Model
51M-1618-10-SP
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-20
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
9e3de440-07bb-484d-88f1-f1b16aad9979

Device Description

CIB Solid 16Dx18Wx10H

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

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00889929027639

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K171140 000

Device Sizes

Type Value Unit Text
Height 10 Millimeter
Width 18 Millimeter
Length 16 Millimeter
Angle 6 degree