The following data is part of a premarket notification filed by Southern Implants (pty) Ltd with the FDA for External Hex Implants.
Device ID | K163634 |
510k Number | K163634 |
Device Name: | External Hex Implants |
Classification | Implant, Endosseous, Root-form |
Applicant | SOUTHERN IMPLANTS (PTY) LTD 1 ALBERT ROAD Irene, ZA 0062 |
Contact | Lauranda Breytenbach |
Correspondent | Linda Schulz 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 | 2016-12-22 |
Decision Date | 2017-11-06 |
Summary: | summary |