Zavation eZspand Interbody System
K-Number: K220581 · 2022-06-02
Device Summary
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. The listed applicant is Zavation Medical Products, LLC. The 510(k) number is K220581.
When did Zavation eZspand Interbody System receive FDA 510(k) clearance?
Zavation eZspand Interbody System received FDA 510(k) clearance on 2022-06-02, under 510(k) number K220581.
Who is the listed applicant for Zavation eZspand Interbody System?
The FDA 510(k) record lists Zavation Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Zavation eZspand Interbody System?
The FDA product code for Zavation eZspand Interbody System is MAX.
Other records listing Zavation Medical Products, LLC 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: MAX)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.