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FDA 510(k)

Zygomatic Implant System

K-Number: K173343 · 2018-02-27

Decision Date2018-02-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Zygomatic Implant System is a medical device manufactured by Southern Implants (Pty), Ltd.. It received FDA 510(k) clearance on 2018-02-27 under approval number K173343. 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 Zygomatic Implant System?

Zygomatic Implant System is a medical device that received FDA 510(k) clearance on 2018-02-27. It is manufactured by Southern Implants (Pty), Ltd.. The 510(k) number is K173343.

When was Zygomatic Implant System approved by the FDA?

Zygomatic Implant System received FDA 510(k) clearance on 2018-02-27, under approval number K173343.

What company makes Zygomatic Implant System?

Zygomatic Implant System is manufactured by Southern Implants (Pty), Ltd..

What is the FDA product code for Zygomatic Implant System?

The FDA product code for Zygomatic Implant System is DZE.

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Official Source

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