The following data is part of a premarket notification filed by Whip-mix Corp. with the FDA for Vericore Implant Abutments.
| Device ID | K082299 |
| 510k Number | K082299 |
| Device Name: | VERICORE IMPLANT ABUTMENTS |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | WHIP-MIX CORP. 361 FARMINGTON AVE. Louisville, KY 40217 |
| Contact | David J Steinbock |
| Correspondent | David J Steinbock WHIP-MIX CORP. 361 FARMINGTON AVE. Louisville, KY 40217 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-12 |
| Decision Date | 2008-11-20 |
| Summary: | summary |