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 a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2017-11-14 under approval 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. It is manufactured by Institut Straumann AG. The 510(k) number is K173410.
When was n!ce for Planmill approved by the FDA?
n!ce for Planmill received FDA 510(k) clearance on 2017-11-14, under approval number K173410.
What company makes n!ce for Planmill?
n!ce for Planmill is manufactured by Institut Straumann AG.
What is the FDA product code for n!ce for Planmill?
The FDA product code for n!ce for Planmill is EIH.
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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.