Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA
K-Number: K220751 · 2022-06-02
ApplicantInstitut Straumann AG
Decision Date2022-06-02
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2022-06-02 under approval number K220751. 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 BLX Temporary Abutment, VITA CAD-Temp, PMMA?
Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA is a medical device that received FDA 510(k) clearance on 2022-06-02. It is manufactured by Institut Straumann AG. The 510(k) number is K220751.
When was Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA approved by the FDA?
Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA received FDA 510(k) clearance on 2022-06-02, under approval number K220751.
What company makes Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA?
Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA?
The FDA product code for Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA is NHA.
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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.