Straumann SC Variobase Abutments
K-Number: K173945 · 2018-10-05
ApplicantInstitut Straumann AG
Decision Date2018-10-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Straumann SC Variobase Abutments is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2018-10-05 under approval number K173945. 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 SC Variobase Abutments?
Straumann SC Variobase Abutments is a medical device that received FDA 510(k) clearance on 2018-10-05. It is manufactured by Institut Straumann AG. The 510(k) number is K173945.
When was Straumann SC Variobase Abutments approved by the FDA?
Straumann SC Variobase Abutments received FDA 510(k) clearance on 2018-10-05, under approval number K173945.
What company makes Straumann SC Variobase Abutments?
Straumann SC Variobase Abutments is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann SC Variobase Abutments?
The FDA product code for Straumann SC Variobase Abutments 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.