Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EZ Plate

K-Number: K173306 · 2018-01-22

Decision Date2018-01-22
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EZ Plate is a medical device manufactured by Zavation Medical Products, LLC. It received FDA 510(k) clearance on 2018-01-22 under approval number K173306. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ Plate?

EZ Plate is a medical device that received FDA 510(k) clearance on 2018-01-22. It is manufactured by Zavation Medical Products, LLC. The 510(k) number is K173306.

When was EZ Plate approved by the FDA?

EZ Plate received FDA 510(k) clearance on 2018-01-22, under approval number K173306.

What company makes EZ Plate?

EZ Plate is manufactured by Zavation Medical Products, LLC.

What is the FDA product code for EZ Plate?

The FDA product code for EZ Plate is KWQ.

Other Devices by Zavation Medical Products, LLC

View all 30 devices →

Related Devices (Code: KWQ)

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.