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FDA 510(k)

Curiteva Anterior Cervical Plate System

K-Number: K181562 · 2018-08-02

ApplicantCuriteva, LLC
Decision Date2018-08-02
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Curiteva Anterior Cervical Plate System is a medical device manufactured by Curiteva, LLC. It received FDA 510(k) clearance on 2018-08-02 under approval number K181562. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Curiteva Anterior Cervical Plate System?

Curiteva Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2018-08-02. It is manufactured by Curiteva, LLC. The 510(k) number is K181562.

When was Curiteva Anterior Cervical Plate System approved by the FDA?

Curiteva Anterior Cervical Plate System received FDA 510(k) clearance on 2018-08-02, under approval number K181562.

What company makes Curiteva Anterior Cervical Plate System?

Curiteva Anterior Cervical Plate System is manufactured by Curiteva, LLC.

What is the FDA product code for Curiteva Anterior Cervical Plate System?

The FDA product code for Curiteva Anterior Cervical Plate System is KWQ.

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Other Devices by Curiteva, LLC

K181589Curiteva Lumbar Interbody Fusion System K181549Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) K181261Curiteva Cervical Interbody Fusion System

Related Devices (Code: KWQ)

K160982Sphynx™Eden Spine, LLC K162638CETRA Anterior Cervical Plate SystemOrthofix, Inc. K162194MEDICREA INTERNATIONAL Anterior Cervical Locking Plate SystemMedicrea International SA K162211AccuFit Lateral Plate SystemPrecision Spine, Inc. K162250FortiBridge Anterior Cervical Plate SystemNanovis Spine, LLC K162664Pyrenees Cervical Plate SystemK2m, 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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