The following data is part of a premarket notification filed by Whip-mix Corp. with the FDA for Vericore Abutment In Zirconia For Implant Systems.
| Device ID | K090976 |
| 510k Number | K090976 |
| Device Name: | VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | WHIP-MIX CORP. 1317 KING STREET Alexandria, VA 22314 |
| Contact | Angela Blackwell |
| Correspondent | Angela Blackwell WHIP-MIX CORP. 1317 KING STREET Alexandria, VA 22314 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-04-06 |
| Decision Date | 2009-06-25 |
| Summary: | summary |