The following data is part of a premarket notification filed by Etgar Medical Instruments, Ltd with the FDA for Etgar Dental Implant System.
Device ID | K161743 |
510k Number | K161743 |
Device Name: | Etgar Dental Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | ETGAR MEDICAL INSTRUMENTS, LTD NORTH INDUSTRIAL AREA Nahariyah, IL 22102 |
Contact | Yehudit Pe’er |
Correspondent | Raymond Kelly LICENSALE INC 57 LAZY BROOK RD Monroe, CT 06468 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-24 |
Decision Date | 2017-04-14 |