The following data is part of a premarket notification filed by Calcitek, Inc. with the FDA for Spline Dental Implant Systems.
| Device ID | K962106 |
| 510k Number | K962106 |
| Device Name: | SPLINE DENTAL IMPLANT SYSTEMS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | CALCITEK, INC. 2320 FARADAY AVE. Carlsbad, CA 92008 -7216 |
| Contact | Donna K Howard |
| Correspondent | Donna K Howard CALCITEK, INC. 2320 FARADAY AVE. Carlsbad, CA 92008 -7216 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-31 |
| Decision Date | 1996-08-29 |
| Summary: | summary |