The following data is part of a premarket notification filed by 3m Espe Ag Dental Products with the FDA for Lava Software.
| Device ID | K062493 |
| 510k Number | K062493 |
| Device Name: | LAVA SOFTWARE |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | 3M ESPE AG DENTAL PRODUCTS ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
| Contact | Sabine Krischer |
| Correspondent | Sabine Krischer 3M ESPE AG DENTAL PRODUCTS ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-25 |
| Decision Date | 2006-11-17 |
| Summary: | summary |