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FDA 510(k)

Cellent Spinal Systems

K-Number: K172826 · 2018-10-10

ApplicantJiangsu Trauhui Medical Instrument Co., Ltd.
Decision Date2018-10-10
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cellent Spinal Systems is a medical device manufactured by Jiangsu Trauhui Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2018-10-10 under approval number K172826. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cellent Spinal Systems?

Cellent Spinal Systems is a medical device that received FDA 510(k) clearance on 2018-10-10. It is manufactured by Jiangsu Trauhui Medical Instrument Co., Ltd.. The 510(k) number is K172826.

When was Cellent Spinal Systems approved by the FDA?

Cellent Spinal Systems received FDA 510(k) clearance on 2018-10-10, under approval number K172826.

What company makes Cellent Spinal Systems?

Cellent Spinal Systems is manufactured by Jiangsu Trauhui Medical Instrument Co., Ltd..

What is the FDA product code for Cellent Spinal Systems?

The FDA product code for Cellent Spinal Systems is NKB.

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Other Devices by Jiangsu Trauhui Medical Instrument Co., Ltd.

K190842Comus Locking Plate systems

Related Devices (Code: NKB)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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