The following data is part of a premarket notification filed by Jeneric/pentron, Inc. with the FDA for Fibrekor Post System.
| Device ID | K983266 |
| 510k Number | K983266 |
| Device Name: | FIBREKOR POST SYSTEM |
| Classification | Post, Root Canal |
| Applicant | JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 -0724 |
| Contact | Murray G Gamberg |
| Correspondent | Murray G Gamberg JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 -0724 |
| Product Code | ELR |
| CFR Regulation Number | 872.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-09-17 |
| Decision Date | 1998-11-09 |