The following data is part of a premarket notification filed by Southern Implants (pty) Ltd with the FDA for Provata Implant System.
Device ID | K180465 |
510k Number | K180465 |
Device Name: | Provata Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | Southern Implants (Pty) Ltd 1 Albert Road Irene, ZA 0062 |
Contact | Lauranda G. Breytenbach |
Correspondent | Kevin A. Thomas PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego, CA 92130 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-02-21 |
Decision Date | 2018-09-06 |