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FDA 510(k)

Implant-One System

K-Number: K173701 · 2018-11-29

Decision Date2018-11-29
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Implant-One System is a medical device manufactured by Implant Logistics, Inc.. It received FDA 510(k) clearance on 2018-11-29 under approval number K173701. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Implant-One System?

Implant-One System is a medical device that received FDA 510(k) clearance on 2018-11-29. It is manufactured by Implant Logistics, Inc.. The 510(k) number is K173701.

When was Implant-One System approved by the FDA?

Implant-One System received FDA 510(k) clearance on 2018-11-29, under approval number K173701.

What company makes Implant-One System?

Implant-One System is manufactured by Implant Logistics, Inc..

What is the FDA product code for Implant-One System?

The FDA product code for Implant-One System is DZE.

Related Clinical Trials

Related PubMed Literature

Other Devices by Implant Logistics, Inc.

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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.