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FDA 510(k)

Multi-unit Abutments for CONELOG

K-Number: K203252 · 2021-03-16

ApplicantBioHorizons Implant Systems, Inc.
Decision Date2021-03-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Multi-unit Abutments for CONELOG is a medical device manufactured by BioHorizons Implant Systems, Inc.. It received FDA 510(k) clearance on 2021-03-16 under approval number K203252. 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 Multi-unit Abutments for CONELOG?

Multi-unit Abutments for CONELOG is a medical device that received FDA 510(k) clearance on 2021-03-16. It is manufactured by BioHorizons Implant Systems, Inc.. The 510(k) number is K203252.

When was Multi-unit Abutments for CONELOG approved by the FDA?

Multi-unit Abutments for CONELOG received FDA 510(k) clearance on 2021-03-16, under approval number K203252.

What company makes Multi-unit Abutments for CONELOG?

Multi-unit Abutments for CONELOG is manufactured by BioHorizons Implant Systems, Inc..

What is the FDA product code for Multi-unit Abutments for CONELOG?

The FDA product code for Multi-unit Abutments for CONELOG is NHA.

Related Clinical Trials

NCT05883202 Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants SUSPENDED

Other Devices by BioHorizons Implant Systems, Inc.

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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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