The following data is part of a premarket notification filed by Whip-mix Corp. with the FDA for Vericore Abutment In Titanium For Implant Systems.
| Device ID | K092857 |
| 510k Number | K092857 |
| Device Name: | VERICORE ABUTMENT IN TITANIUM FOR IMPLANT SYSTEMS |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | WHIP-MIX CORP. 361 FARMINGTON AVE. P.O. BOX 17183 Louisville, KY 40209 |
| Contact | Stuart Steinbock |
| Correspondent | Stuart Steinbock WHIP-MIX CORP. 361 FARMINGTON AVE. P.O. BOX 17183 Louisville, KY 40209 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-16 |
| Decision Date | 2010-03-04 |
| Summary: | summary |