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FDA 510(k)

Straumann Variobase for Bridge/Bar Cylindrical

K-Number: K173968 · 2018-07-17

ApplicantInstitut Straumann AG
Decision Date2018-07-17
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Straumann Variobase for Bridge/Bar Cylindrical is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2018-07-17 under approval number K173968. 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 Straumann Variobase for Bridge/Bar Cylindrical?

Straumann Variobase for Bridge/Bar Cylindrical is a medical device that received FDA 510(k) clearance on 2018-07-17. It is manufactured by Institut Straumann AG. The 510(k) number is K173968.

When was Straumann Variobase for Bridge/Bar Cylindrical approved by the FDA?

Straumann Variobase for Bridge/Bar Cylindrical received FDA 510(k) clearance on 2018-07-17, under approval number K173968.

What company makes Straumann Variobase for Bridge/Bar Cylindrical?

Straumann Variobase for Bridge/Bar Cylindrical is manufactured by Institut Straumann AG.

What is the FDA product code for Straumann Variobase for Bridge/Bar Cylindrical?

The FDA product code for Straumann Variobase for Bridge/Bar Cylindrical 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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