Matrixx System

FDA UDI

Class II (US FDA UDI)

by Nexxt Spine Llc

Identity

Trade Name: Matrixx System FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: Lateral, 18Wx50Lx14H 20° FDA UDI
Model / Reference: 62-1850-14-20-SP FDA UDI
Description: Lateral, 18Wx50Lx14H 20° FDA UDI

Identifiers

Primary DI / UDI-DI: 00889929055380 FDA UDI
510(k) Number: K200969 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 50 Millimeter FDA UDI
Height — 14 Millimeter FDA UDI
Depth — 18 Millimeter FDA UDI
Angle — 20 degree FDA UDI

Category: Metallic spinal interbody fusion cage

The Matrixx System is a cutting-edge, patented spinal interbody fusion cage designed to promote bone fusion between two contiguous vertebral bodies. This innovative device is intended for the treatment of degenerative disc disease and offers a unique combination of mechanical stability and sufficient space for therapeutic spinal bone fusion.

Similar devices

Also classified as Metallic spinal interbody fusion cage.

KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
CoRoent — Nuvasive, Inc. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
MectaLIF 3D — Medacta International · Class II
PILLAR TL — Orthofix US LLC · Class II
Solar™ Interbody Fusion System — Degen Medical · Class II
Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II

Cleared under the same submission

K200969 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Nexxt Spine Llc

Sources (1)

FDA UDI e3a0deb8-8da5-4c44-b595-7f86d55522ce 36 fields · synced Jul 22, 2026