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FDA 510(k)

Curiteva Thoracolumbar Plate System

K-Number: K233360 · 2024-02-29

ApplicantCuriteva, Inc.
Decision Date2024-02-29
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Curiteva Thoracolumbar Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Curiteva, Inc.. It received FDA 510(k) clearance on 2024-02-29 under 510(k) number K233360. 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 Thoracolumbar Plate System?

Curiteva Thoracolumbar Plate System is a medical device that received FDA 510(k) clearance on 2024-02-29. The listed applicant is Curiteva, Inc.. The 510(k) number is K233360.

When did Curiteva Thoracolumbar Plate System receive FDA 510(k) clearance?

Curiteva Thoracolumbar Plate System received FDA 510(k) clearance on 2024-02-29, under 510(k) number K233360.

Who is the listed applicant for Curiteva Thoracolumbar Plate System?

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

What is the FDA product code for Curiteva Thoracolumbar Plate System?

The FDA product code for Curiteva Thoracolumbar Plate System is KWQ.

Other records listing Curiteva, Inc. as applicant

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K252205Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF SystemK254061Curiteva Porous PEEK Cervical Interbody Fusion SystemK250845Curiteva Porous PEEK Standalone ALIF SystemK243137Curiteva Porous PEEK Laminoplasty SystemK233744Curiteva Porous PEEK Lumbar Interbody Fusion SystemK231232Curiteva Laminoplasty System

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Related Devices (Code: KWQ)

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.

K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLCK260015ANTERIS Thoracolumbar Plate SystemSpineCraft

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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