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 |