The following data is part of a premarket notification filed by Southern Implants (pty) Ltd with the FDA for Inversa Implants.
Device ID | K181850 |
510k Number | K181850 |
Device Name: | Inversa Implants |
Classification | Implant, Endosseous, Root-form |
Applicant | Southern Implants (Pty) Ltd 1 Albert Road Irene, ZA 0062 |
Contact | Lauranda 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 | 2018-07-11 |
Decision Date | 2018-11-14 |
Summary: | summary |