The following data is part of a premarket notification filed by Implant Direct Llc with the FDA for Replus Dental Implants (ha).
| Device ID | K073161 |
| 510k Number | K073161 |
| Device Name: | REPLUS DENTAL IMPLANTS (HA) |
| Classification | Implant, Endosseous, Root-form |
| Applicant | IMPLANT DIRECT LLC 27030 MALIBU HILLS RD. Calabasas Hills, CA 91301 |
| Contact | Thomas Gottenbos |
| Correspondent | Thomas Gottenbos IMPLANT DIRECT LLC 27030 MALIBU HILLS RD. Calabasas Hills, CA 91301 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-11-09 |
| Decision Date | 2008-03-07 |
| Summary: | summary |