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FDA 510(k)

NuVasive CoRoent Small Interlock System

K-Number: K192582 · 2019-11-13

ApplicantNu Vasive, Incorporated
Decision Date2019-11-13
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NuVasive CoRoent Small Interlock System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2019-11-13 under approval number K192582. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NuVasive CoRoent Small Interlock System?

NuVasive CoRoent Small Interlock System is a medical device that received FDA 510(k) clearance on 2019-11-13. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K192582.

When was NuVasive CoRoent Small Interlock System approved by the FDA?

NuVasive CoRoent Small Interlock System received FDA 510(k) clearance on 2019-11-13, under approval number K192582.

What company makes NuVasive CoRoent Small Interlock System?

NuVasive CoRoent Small Interlock System is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for NuVasive CoRoent Small Interlock System?

The FDA product code for NuVasive CoRoent Small Interlock System is OVE.

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Related PubMed Literature

PMID: 42168293 Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling. Scientific reports (2026)

Other Devices by Nu Vasive, Incorporated

K162138NuVasive CoRoent Small Ti-C System K161014NuVasive® Reline® System K161442NuVasive® CoRoent® Small Interlock™ System K161230NuVasive Lumbar Interbody Implants K161265NuVasive® VersaTie System K153105MLX™ - Medial Lateral Expandable Lumbar Interbody System

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Related Devices (Code: OVE)

K162531STERISPINE CCSafe Orthopaedics K162944Irix-C Cervical Integrated Fusion SystemX-Spine Systems, Inc. K160313Xenco Medical Cervical Interbody SystemXenco Medical, LLC K161442NuVasive® CoRoent® Small Interlock™ SystemNu Vasive, Incorporated K161081SeaSpine Shoreline ACS - Anterior Cervical Standalone SystemSeaSpine Orthopedics Corporation K160066Pro-Link® Stand-Alone Cervical Spacer SystemLife Spine, 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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