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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
Corpectomy, 12Dx14Wx41H 0° FDA UDI
Model / Reference
53-1214-41-0-SP FDA UDI
Description
Corpectomy, 12Dx14Wx41H 0° FDA UDI

Identifiers

Primary DI / UDI-DI
00889929064757 FDA UDI
510(k) Number
K193412 FDA UDI
FDA Product Code
MQP FDA UDI
PLR FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Depth — 12 Millimeter FDA UDI
Width — 14 Millimeter FDA UDI
Height — 41 Millimeter FDA UDI
Angle — 0 degree FDA UDI

Category: Metallic spinal interbody fusion cage

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

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

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 9c09841d-6921-4984-938f-ba37be4dedd4 36 fields · synced Jun 8, 2026