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FDA 510(k)

IPS e.max® Press Abutment Solutions for Viteo Base Ti

K-Number: K160798 · 2016-12-15

ApplicantIvoclar Vivadent, AG
Decision Date2016-12-15
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IPS e.max® Press Abutment Solutions for Viteo Base Ti is a medical device manufactured by Ivoclar Vivadent, AG. It received FDA 510(k) clearance on 2016-12-15 under approval number K160798. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPS e.max® Press Abutment Solutions for Viteo Base Ti?

IPS e.max® Press Abutment Solutions for Viteo Base Ti is a medical device that received FDA 510(k) clearance on 2016-12-15. It is manufactured by Ivoclar Vivadent, AG. The 510(k) number is K160798.

When was IPS e.max® Press Abutment Solutions for Viteo Base Ti approved by the FDA?

IPS e.max® Press Abutment Solutions for Viteo Base Ti received FDA 510(k) clearance on 2016-12-15, under approval number K160798.

What company makes IPS e.max® Press Abutment Solutions for Viteo Base Ti?

IPS e.max® Press Abutment Solutions for Viteo Base Ti is manufactured by Ivoclar Vivadent, AG.

What is the FDA product code for IPS e.max® Press Abutment Solutions for Viteo Base Ti?

The FDA product code for IPS e.max® Press Abutment Solutions for Viteo Base Ti is NHA.

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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.

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