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FDA 510(k)

NEXXT MATRIXX Stand Alone ALIF System

K-Number: K202230 · 2020-12-15

ApplicantNexxt Spine, LLC
Decision Date2020-12-15
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEXXT MATRIXX Stand Alone ALIF System is the device name listed in this FDA 510(k) record. The listed applicant is Nexxt Spine, LLC. It received FDA 510(k) clearance on 2020-12-15 under 510(k) 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. The listed applicant is Nexxt Spine, LLC. The 510(k) number is K202230.

When did NEXXT MATRIXX Stand Alone ALIF System receive FDA 510(k) clearance?

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

Who is the listed applicant for NEXXT MATRIXX Stand Alone ALIF System?

The FDA 510(k) record lists Nexxt Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Nexxt Spine, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243838NEXXT MATRIXX® SI SystemK240690STRUXXURE® MCS Anterior Cervical Plate SystemK231799INERTIA® CONNEXX™ Modular Pedicle Screw SystemK221905INERTIA CONNEXX Modular Pedicle Screw SystemK220291NEXXT SPINE NAVIGATION SystemK202192STRUXXURE®-L and STRUXXURE®-A Plate System

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Related Devices (Code: OVD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261408SABER-XA SystemElevation SpineK261809Interwedge® Standalone LateralFoundation Surgical GroupK261353Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar Anchor SystemKyocera Medical Technologies, Inc.K260810Anteralign LS coverplateTyber Medical, LLCK254202MectaLIF 3D Metal AnteriorMedacta International S.A.K253401SCRIPT™ Implant SystemGlobus Medical, Inc.

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.

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