Straumann Immediate Temporary Abutments
K-Number: K201681 · 2021-03-18
Device Summary
Frequently Asked Questions
What is the Straumann Immediate Temporary Abutments?
Straumann Immediate Temporary Abutments is a medical device that received FDA 510(k) clearance on 2021-03-18. It is manufactured by Institut Straumann AG. The 510(k) number is K201681.
When was Straumann Immediate Temporary Abutments approved by the FDA?
Straumann Immediate Temporary Abutments received FDA 510(k) clearance on 2021-03-18, under approval number K201681.
What company makes Straumann Immediate Temporary Abutments?
Straumann Immediate Temporary Abutments is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann Immediate Temporary Abutments?
The FDA product code for Straumann Immediate Temporary Abutments is NHA.
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Other Devices by Institut Straumann AG
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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.