The following data is part of a premarket notification filed by Zimmer Dental, Inc. with the FDA for Zimmer Zfx Abutment For Zimmer 3.1mmd Implant System.
| Device ID | K142572 |
| 510k Number | K142572 |
| Device Name: | Zimmer Zfx Abutment For Zimmer 3.1mmD Implant System |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | Zimmer Dental, Inc. 1900 Aston Ave. Carldsbad, CA 92008 |
| Contact | Christina Boydston |
| Correspondent | Christina Boydston Zimmer Dental, Inc. 1900 Aston Ave. Carldsbad, CA 92008 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-12 |
| Decision Date | 2015-01-21 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024344464 | K142572 | 000 |