FDA 510(k)

Matrixx System

K-Number: K171140 · 2017-08-22

Decision Date2017-08-22

Product CodeODP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Matrixx System is a medical device manufactured by Nexxt Spine, LLC. It received FDA 510(k) clearance on 2017-08-22 under approval number K171140. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Matrixx System?

Matrixx System is a medical device that received FDA 510(k) clearance on 2017-08-22. It is manufactured by Nexxt Spine, LLC. The 510(k) number is K171140.

When was Matrixx System approved by the FDA?

Matrixx System received FDA 510(k) clearance on 2017-08-22, under approval number K171140.

What company makes Matrixx System?

Matrixx System is manufactured by Nexxt Spine, LLC.

What is the FDA product code for Matrixx System?

The FDA product code for Matrixx System is ODP.

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Related Devices (Code: ODP)

K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.