The following data is part of a premarket notification filed by Zimmer Dental Inc. with the FDA for Zimmer Dental Hex-lock Prepared Abutment (straight & Angled).
| Device ID | K052600 |
| 510k Number | K052600 |
| Device Name: | ZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED) |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | ZIMMER DENTAL INC. 1900 ASTON AVE. Carlsbad, CA 92008 -7308 |
| Contact | Erin Mcvey |
| Correspondent | Erin Mcvey 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 | 2005-09-21 |
| Decision Date | 2005-10-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024020900 | K052600 | 000 |
| 00889024020795 | K052600 | 000 |
| 00889024020788 | K052600 | 000 |
| 00889024020771 | K052600 | 000 |
| 00889024020764 | K052600 | 000 |
| 00889024020757 | K052600 | 000 |
| 00889024020740 | K052600 | 000 |
| 00889024020733 | K052600 | 000 |
| 00889024020726 | K052600 | 000 |
| 00889024020801 | K052600 | 000 |
| 00889024020818 | K052600 | 000 |
| 00889024020894 | K052600 | 000 |
| 00889024020887 | K052600 | 000 |
| 00889024020870 | K052600 | 000 |
| 00889024020863 | K052600 | 000 |
| 00889024020856 | K052600 | 000 |
| 00889024020849 | K052600 | 000 |
| 00889024020832 | K052600 | 000 |
| 00889024020825 | K052600 | 000 |
| 00889024020719 | K052600 | 000 |