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FDA 510(k)

Ti3Z Cervical Interbody System

K-Number: K202398 · 2021-01-29

Decision Date2021-01-29
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Ti3Z Cervical Interbody System is the device name listed in this FDA 510(k) record. The listed applicant is Zavation Medical Products, LLC. It received FDA 510(k) clearance on 2021-01-29 under 510(k) number K202398. 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 Ti3Z Cervical Interbody System?

Ti3Z Cervical Interbody System is a medical device that received FDA 510(k) clearance on 2021-01-29. The listed applicant is Zavation Medical Products, LLC. The 510(k) number is K202398.

When did Ti3Z Cervical Interbody System receive FDA 510(k) clearance?

Ti3Z Cervical Interbody System received FDA 510(k) clearance on 2021-01-29, under 510(k) number K202398.

Who is the listed applicant for Ti3Z Cervical 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 Ti3Z Cervical Interbody System?

The FDA product code for Ti3Z Cervical Interbody System is ODP.

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.

View all 31 devices →

Related Devices (Code: ODP)

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.