The following data is part of a premarket notification filed by Dentsply Sirona with the FDA for Multibase Abutments Ev And Atlantis Suprastructures.
| Device ID | K163350 |
| 510k Number | K163350 |
| Device Name: | Multibase Abutments EV And ATLANTIS Suprastructures |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | DENTSPLY SIRONA 221 WEST PHILADELPHIA STREET SUITE 60 York, PA 17404 |
| Contact | Karl Nittinger |
| Correspondent | Karl Nittinger DENTSPLY SIRONA 221 WEST PHILADELPHIA STREET SUITE 60 York, PA 17404 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-11-30 |
| Decision Date | 2017-03-31 |
| Summary: | summary |