The following data is part of a premarket notification filed by Implant Center Of The Palm Beaches with the FDA for Kis-- Four Hole Cylinder.
Device ID | K953139 |
510k Number | K953139 |
Device Name: | KIS-- FOUR HOLE CYLINDER |
Classification | Implant, Endosseous, Root-form |
Applicant | IMPLANT CENTER OF THE PALM BEACHES 824 US HWY I, STE. 370 N. Palm Beach, FL 33408 |
Contact | Jack T Krauser |
Correspondent | Jack T Krauser IMPLANT CENTER OF THE PALM BEACHES 824 US HWY I, STE. 370 N. 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 | 1995-07-06 |
Decision Date | 1995-09-13 |