ATLANTIS Abutment for MIS Conical Connection Implants
K-Number: K193529 · 2020-03-05
ApplicantDentsply Sirona
Decision Date2020-03-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
ATLANTIS Abutment for MIS Conical Connection Implants is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2020-03-05 under approval number K193529. 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 Abutment for MIS Conical Connection Implants?
ATLANTIS Abutment for MIS Conical Connection Implants is a medical device that received FDA 510(k) clearance on 2020-03-05. It is manufactured by Dentsply Sirona. The 510(k) number is K193529.
When was ATLANTIS Abutment for MIS Conical Connection Implants approved by the FDA?
ATLANTIS Abutment for MIS Conical Connection Implants received FDA 510(k) clearance on 2020-03-05, under approval number K193529.
What company makes ATLANTIS Abutment for MIS Conical Connection Implants?
ATLANTIS Abutment for MIS Conical Connection Implants is manufactured by Dentsply Sirona.
What is the FDA product code for ATLANTIS Abutment for MIS Conical Connection Implants?
The FDA product code for ATLANTIS Abutment for MIS Conical Connection Implants 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.