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FDA 510(k)

Cellent Spinal Systems

K-Number: K172826 · 2018-10-10

Decision Date2018-10-10
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cellent Spinal Systems is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Trauhui Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2018-10-10 under 510(k) 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. The listed applicant is Jiangsu Trauhui Medical Instrument Co., Ltd.. The 510(k) number is K172826.

When did Cellent Spinal Systems receive FDA 510(k) clearance?

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

Who is the listed applicant for Cellent Spinal Systems?

The FDA 510(k) record lists Jiangsu Trauhui Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cellent Spinal Systems?

The FDA product code for Cellent Spinal Systems is NKB.

Other records listing Jiangsu Trauhui Medical Instrument Co., Ltd. as applicant

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.

Related Devices (Code: NKB)

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.

Official Source

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