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FDA 510(k)

Zavation eZspand Interbody System

K-Number: K220581 · 2022-06-02

Decision Date2022-06-02
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zavation eZspand Interbody System is a medical device manufactured by Zavation Medical Products, LLC. It received FDA 510(k) clearance on 2022-06-02 under approval number K220581. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zavation eZspand Interbody System?

Zavation eZspand Interbody System is a medical device that received FDA 510(k) clearance on 2022-06-02. It is manufactured by Zavation Medical Products, LLC. The 510(k) number is K220581.

When was Zavation eZspand Interbody System approved by the FDA?

Zavation eZspand Interbody System received FDA 510(k) clearance on 2022-06-02, under approval number K220581.

What company makes Zavation eZspand Interbody System?

Zavation eZspand Interbody System is manufactured by Zavation Medical Products, LLC.

What is the FDA product code for Zavation eZspand Interbody System?

The FDA product code for Zavation eZspand Interbody System is MAX.

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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.