The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Filpost.
| Device ID | K896928 |
| 510k Number | K896928 |
| Device Name: | FILPOST |
| Classification | Post, Root Canal |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Gary Severance |
| Correspondent | Gary Severance IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | ELR |
| CFR Regulation Number | 872.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-12-11 |
| Decision Date | 1990-03-05 |