Multi-unit Abutments For CONELOG

Abutment, Implant, Dental, Endosseous

BioHorizons Implant Systems, Inc.

The following data is part of a premarket notification filed by Biohorizons Implant Systems, Inc. with the FDA for Multi-unit Abutments For Conelog.

Pre-market Notification Details

Device IDK203252
510k NumberK203252
Device Name:Multi-unit Abutments For CONELOG
ClassificationAbutment, Implant, Dental, Endosseous
Applicant BioHorizons Implant Systems, Inc. 2300 Riverchase Center Birmingham,  AL  35244
ContactBill Hornbuckle
CorrespondentFloyd G Larson
PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego,  CA  92130
Product CodeNHA  
CFR Regulation Number872.3630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-11-04
Decision Date2021-03-16
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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