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FDA 510(k)

ZSFab Cervical Interbody System

K-Number: K232150 · 2023-08-18

ApplicantZsfab, Inc.
Decision Date2023-08-18
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZSFab Cervical Interbody System is a medical device manufactured by Zsfab, Inc.. It received FDA 510(k) clearance on 2023-08-18 under approval number K232150. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZSFab Cervical Interbody System?

ZSFab Cervical Interbody System is a medical device that received FDA 510(k) clearance on 2023-08-18. It is manufactured by Zsfab, Inc.. The 510(k) number is K232150.

When was ZSFab Cervical Interbody System approved by the FDA?

ZSFab Cervical Interbody System received FDA 510(k) clearance on 2023-08-18, under approval number K232150.

What company makes ZSFab Cervical Interbody System?

ZSFab Cervical Interbody System is manufactured by Zsfab, Inc..

What is the FDA product code for ZSFab Cervical Interbody System?

The FDA product code for ZSFab Cervical Interbody System is ODP.

Related Clinical Trials

Other Devices by Zsfab, Inc.

Related Devices (Code: ODP)

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.