The following data is part of a premarket notification filed by Ceramed Corp. with the FDA for Permaridge Hydroxylapatite Matrix.
| Device ID | K960349 |
| 510k Number | K960349 |
| Device Name: | PERMARIDGE HYDROXYLAPATITE MATRIX |
| Classification | Prosthesis, Chin, Internal |
| Applicant | CERAMED CORP. 12860 WEST CEDAR DR., STE. 110 Lakewood, CO 80228 |
| Contact | Barbara A Watson |
| Correspondent | Barbara A Watson CERAMED CORP. 12860 WEST CEDAR DR., STE. 110 Lakewood, CO 80228 |
| Product Code | FWP |
| CFR Regulation Number | 878.3550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-25 |
| Decision Date | 1996-03-13 |
| Summary: | summary |