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FDA 510(k)

VITA VIONIC Bond

K-Number: K191926 · 2020-01-29

ApplicantVita Zanhnfabrik H. Rauter GmbH Co.
Decision Date2020-01-29
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITA VIONIC Bond is a medical device manufactured by Vita Zanhnfabrik H. Rauter GmbH Co.. It received FDA 510(k) clearance on 2020-01-29 under approval number K191926. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA VIONIC Bond?

VITA VIONIC Bond is a medical device that received FDA 510(k) clearance on 2020-01-29. It is manufactured by Vita Zanhnfabrik H. Rauter GmbH Co.. The 510(k) number is K191926.

When was VITA VIONIC Bond approved by the FDA?

VITA VIONIC Bond received FDA 510(k) clearance on 2020-01-29, under approval number K191926.

What company makes VITA VIONIC Bond?

VITA VIONIC Bond is manufactured by Vita Zanhnfabrik H. Rauter GmbH Co..

What is the FDA product code for VITA VIONIC Bond?

The FDA product code for VITA VIONIC Bond is EBI.

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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.

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