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FDA 510(k)

n!ce for Planmill

K-Number: K173410 · 2017-11-14

ApplicantInstitut Straumann AG
Decision Date2017-11-14
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

n!ce for Planmill 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 2017-11-14 under 510(k) number K173410. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the n!ce for Planmill?

n!ce for Planmill is a medical device that received FDA 510(k) clearance on 2017-11-14. The listed applicant is Institut Straumann AG. The 510(k) number is K173410.

When did n!ce for Planmill receive FDA 510(k) clearance?

n!ce for Planmill received FDA 510(k) clearance on 2017-11-14, under 510(k) number K173410.

Who is the listed applicant for n!ce for Planmill?

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 n!ce for Planmill?

The FDA product code for n!ce for Planmill is EIH.

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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