Provata Implant System

Implant, Endosseous, Root-form

Southern Implants (Pty) Ltd

The following data is part of a premarket notification filed by Southern Implants (pty) Ltd with the FDA for Provata Implant System.

Pre-market Notification Details

Device IDK180465
510k NumberK180465
Device Name:Provata Implant System
ClassificationImplant, Endosseous, Root-form
Applicant Southern Implants (Pty) Ltd 1 Albert Road Irene,  ZA 0062
ContactLauranda G. Breytenbach
CorrespondentKevin A. Thomas
PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego,  CA  92130
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-02-21
Decision Date2018-09-06

NIH GUDID Devices

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