FDA 510(k)

NEXXT MATRIXX Stand Alone ALIF System

K-Number: K202230 · 2020-12-15

Decision Date2020-12-15

Product CodeOVD

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

NEXXT MATRIXX Stand Alone ALIF System is a medical device manufactured by Nexxt Spine, LLC. It received FDA 510(k) clearance on 2020-12-15 under approval number K202230. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXXT MATRIXX Stand Alone ALIF System?

NEXXT MATRIXX Stand Alone ALIF System is a medical device that received FDA 510(k) clearance on 2020-12-15. It is manufactured by Nexxt Spine, LLC. The 510(k) number is K202230.

When was NEXXT MATRIXX Stand Alone ALIF System approved by the FDA?

NEXXT MATRIXX Stand Alone ALIF System received FDA 510(k) clearance on 2020-12-15, under approval number K202230.

What company makes NEXXT MATRIXX Stand Alone ALIF System?

NEXXT MATRIXX Stand Alone ALIF System is manufactured by Nexxt Spine, LLC.

What is the FDA product code for NEXXT MATRIXX Stand Alone ALIF System?

The FDA product code for NEXXT MATRIXX Stand Alone ALIF System is OVD.

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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.