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FDA 510(k)

Straumann Variobase Abutments

K-Number: K170356 · 2017-06-07

Decision Date2017-06-07
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Straumann Variobase Abutments 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 2017-06-07 under 510(k) number K170356. 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 Abutments?

Straumann Variobase Abutments is a medical device that received FDA 510(k) clearance on 2017-06-07. The listed applicant is Institut Straumann AG. The 510(k) number is K170356.

When did Straumann Variobase Abutments receive FDA 510(k) clearance?

Straumann Variobase Abutments received FDA 510(k) clearance on 2017-06-07, under 510(k) number K170356.

Who is the listed applicant for Straumann Variobase Abutments?

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 Abutments?

The FDA product code for Straumann Variobase Abutments is NHA.

Other records listing Institut Straumann AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: NHA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.