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FDA 510(k)

NuVasive Cohere ALIF System Intervertebral Body Fusion Device

K-Number: K221751 · 2022-10-21

ApplicantNu Vasive, Incorporated
Decision Date2022-10-21
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive Cohere ALIF System Intervertebral Body Fusion Device is the device name listed in this FDA 510(k) record. The listed applicant is Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K221751. 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 NuVasive Cohere ALIF System Intervertebral Body Fusion Device?

NuVasive Cohere ALIF System Intervertebral Body Fusion Device is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K221751.

When did NuVasive Cohere ALIF System Intervertebral Body Fusion Device receive FDA 510(k) clearance?

NuVasive Cohere ALIF System Intervertebral Body Fusion Device received FDA 510(k) clearance on 2022-10-21, under 510(k) number K221751.

Who is the listed applicant for NuVasive Cohere ALIF System Intervertebral Body Fusion Device?

The FDA 510(k) record lists Nu Vasive, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NuVasive Cohere ALIF System Intervertebral Body Fusion Device?

The FDA product code for NuVasive Cohere ALIF System Intervertebral Body Fusion Device is OVD.

Related Clinical Trials

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.

NCT07414745MDT-0123 Japan StudyRECRUITING

Other records listing Nu Vasive, Incorporated 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.

K231735NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody SystemK230894NuVasive Modulus ALIF SystemK230989Rod Registration FrameK223181NuVasive Reline SystemK221388NuVasive Reline Cervical SystemK220478NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody 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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