Multibase Abutments EV and ATLANTIS Suprastructures
K-Number: K163350 · 2017-03-31
ApplicantDentsply Sirona
Decision Date2017-03-31
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Multibase Abutments EV and ATLANTIS Suprastructures is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2017-03-31 under approval number K163350. 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 Multibase Abutments EV and ATLANTIS Suprastructures?
Multibase Abutments EV and ATLANTIS Suprastructures is a medical device that received FDA 510(k) clearance on 2017-03-31. It is manufactured by Dentsply Sirona. The 510(k) number is K163350.
When was Multibase Abutments EV and ATLANTIS Suprastructures approved by the FDA?
Multibase Abutments EV and ATLANTIS Suprastructures received FDA 510(k) clearance on 2017-03-31, under approval number K163350.
What company makes Multibase Abutments EV and ATLANTIS Suprastructures?
Multibase Abutments EV and ATLANTIS Suprastructures is manufactured by Dentsply Sirona.
What is the FDA product code for Multibase Abutments EV and ATLANTIS Suprastructures?
The FDA product code for Multibase Abutments EV and 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.