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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 a medical device manufactured by Curiteva, Inc.. It received FDA 510(k) clearance on 2024-02-29 under approval 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. It is manufactured by Curiteva, Inc.. The 510(k) number is K233360.

When was Curiteva Thoracolumbar Plate System approved by the FDA?

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

What company makes Curiteva Thoracolumbar Plate System?

Curiteva Thoracolumbar Plate System is manufactured by Curiteva, Inc..

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

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

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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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