Atlantis suprastructures
K-Number: K193064 · 2020-03-03
ApplicantDentsply Sirona, Inc.
Decision Date2020-03-03
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Atlantis suprastructures is a medical device manufactured by Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2020-03-03 under approval number K193064. 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 Atlantis suprastructures?
Atlantis suprastructures is a medical device that received FDA 510(k) clearance on 2020-03-03. It is manufactured by Dentsply Sirona, Inc.. The 510(k) number is K193064.
When was Atlantis suprastructures approved by the FDA?
Atlantis suprastructures received FDA 510(k) clearance on 2020-03-03, under approval number K193064.
What company makes Atlantis suprastructures?
Atlantis suprastructures is manufactured by Dentsply Sirona, Inc..
What is the FDA product code for Atlantis suprastructures?
The FDA product code for Atlantis suprastructures 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.