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FDA 510(k)

ATLANTIS Abutment for CONELOG implant

K-Number: K161030 · 2016-08-26

ApplicantDentsply Sirona
Decision Date2016-08-26
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ATLANTIS Abutment for CONELOG implant is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2016-08-26 under approval number K161030. 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 CONELOG implant?

ATLANTIS Abutment for CONELOG implant is a medical device that received FDA 510(k) clearance on 2016-08-26. It is manufactured by Dentsply Sirona. The 510(k) number is K161030.

When was ATLANTIS Abutment for CONELOG implant approved by the FDA?

ATLANTIS Abutment for CONELOG implant received FDA 510(k) clearance on 2016-08-26, under approval number K161030.

What company makes ATLANTIS Abutment for CONELOG implant?

ATLANTIS Abutment for CONELOG implant is manufactured by Dentsply Sirona.

What is the FDA product code for ATLANTIS Abutment for CONELOG implant?

The FDA product code for ATLANTIS Abutment for CONELOG implant is NHA.

Related Clinical Trials

NCT07246499 Multicentre Study on the Impact of Transmucosal Abutment Surface Characteristics on Peri-implant Tissues. ACTIVE_NOT_RECRUITING NCT05883202 Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants SUSPENDED NCT06636136 Transtibial Osseointegration RECRUITING

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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.

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