The following data is part of a premarket notification filed by Coltene/whaledent Inc. with the FDA for Parapost Fiber White.
| Device ID | K000311 |
| 510k Number | K000311 |
| Device Name: | PARAPOST FIBER WHITE |
| Classification | Post, Root Canal |
| Applicant | COLTENE/WHALEDENT INC. 750 CORPORATE DR. Mahwah, NJ 07430 -2009 |
| Contact | H.j. Vogelstein |
| Correspondent | H.j. Vogelstein COLTENE/WHALEDENT INC. 750 CORPORATE DR. Mahwah, NJ 07430 -2009 |
| Product Code | ELR |
| CFR Regulation Number | 872.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-02-01 |
| Decision Date | 2000-03-14 |