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Matrixx System

FDA UDI

Class I (US FDA UDI)

by Nexxt Spine Llc

Identity

Trade Name
Matrixx System FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Matrixx Cervical Rasp, 6°, No Stop, 16x18x07mm FDA UDI
Model / Reference
I50-RA68-07-NS FDA UDI
Description
Matrixx Cervical Rasp, 6°, No Stop, 16x18x07mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889929031650 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI
Width — 18 Millimeter FDA UDI
Height — 7 Millimeter FDA UDI
Angle — 6 degree FDA UDI

Category: General internal orthopaedic fixation system implantation kit

Matrixx System by Nexxt Spine Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nexxt Spine Llc

Sources (1)

  • FDA UDI 753f6612-133e-4480-b126-8f3848a602d8 35 fields · synced May 31, 2026