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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 the device name listed in this FDA 510(k) record. The listed applicant is Institut Straumann AG. It received FDA 510(k) clearance on 2018-07-17 under 510(k) 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. The listed applicant is Institut Straumann AG. The 510(k) number is K173968.

When did Straumann Variobase for Bridge/Bar Cylindrical receive FDA 510(k) clearance?

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

Who is the listed applicant for Straumann Variobase for Bridge/Bar Cylindrical?

The FDA 510(k) record lists Institut Straumann AG as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Institut Straumann AG as applicant

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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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