The following data is part of a premarket notification filed by Zimmer Dental Inc. with the FDA for Zimmer Angled Contour Zirconia Abutment.
| Device ID | K083474 |
| 510k Number | K083474 |
| Device Name: | ZIMMER ANGLED CONTOUR ZIRCONIA ABUTMENT |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | ZIMMER DENTAL INC. 1900 ASTON AVE. Carlsbad, CA 92008 -7308 |
| Contact | William Fisher |
| Correspondent | William Fisher ZIMMER DENTAL INC. 1900 ASTON AVE. Carlsbad, CA 92008 -7308 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-11-24 |
| Decision Date | 2008-12-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024021556 | K083474 | 000 |
| 00889024021549 | K083474 | 000 |
| 00889024021518 | K083474 | 000 |
| 00889024021501 | K083474 | 000 |