The following data is part of a premarket notification filed by The Implant Center Of The Palm Beaches with the FDA for Kis Mt3.
| Device ID | K960110 |
| 510k Number | K960110 |
| Device Name: | KIS MT3 |
| Classification | Implant, Endosseous, Root-form |
| Applicant | THE IMPLANT CENTER OF THE PALM BEACHES 824 U.S HIGHWAY 1 SUITE 370 North Palm Beach, FL 33408 |
| Contact | Jack T Krauser |
| Correspondent | Jack T Krauser THE IMPLANT CENTER OF THE PALM BEACHES 824 U.S HIGHWAY 1 SUITE 370 North Palm Beach, FL 33408 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-11 |
| Decision Date | 1996-03-20 |
| Summary: | summary |