The following data is part of a premarket notification filed by Cox-uphuff Intl. with the FDA for Ligature Carrier/packer, Hydroxylapatite.
| Device ID | K874342 |
| 510k Number | K874342 |
| Device Name: | LIGATURE CARRIER/PACKER, HYDROXYLAPATITE |
| Classification | Carrier, Ligature |
| Applicant | COX-UPHUFF INTL. P.O. BOX 40288 Santa Barbara, CA 93140 |
| Contact | David J Schuessler |
| Correspondent | David J Schuessler COX-UPHUFF INTL. P.O. BOX 40288 Santa Barbara, CA 93140 |
| Product Code | GEJ |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-20 |
| Decision Date | 1987-11-13 |