The following data is part of a premarket notification filed by Kavo America with the FDA for Kavo Everest Titanblank.
| Device ID | K024214 |
| 510k Number | K024214 |
| Device Name: | KAVO EVEREST TITANBLANK |
| Classification | Alloy, Metal, Base |
| Applicant | KAVO AMERICA 340 EAST MAIN ST. Lake Zurich, IL 60047 |
| Contact | John R Franz |
| Correspondent | John R Franz KAVO AMERICA 340 EAST MAIN ST. Lake Zurich, IL 60047 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-12-20 |
| Decision Date | 2003-03-12 |
| Summary: | summary |