The following data is part of a premarket notification filed by Osstem Implant Co., Ltd. with the FDA for Ss Sa Fixture.
| Device ID | K163557 |
| 510k Number | K163557 |
| Device Name: | SS SA Fixture |
| Classification | Implant, Endosseous, Root-form |
| Applicant | OSSTEM IMPLANT Co., Ltd. 66-16, Bansong-ro 513beon-gil, Haeundae-gu Busan, KR 612-070 |
| Contact | Mr. Heekwon |
| Correspondent | David Kim HiOSSEN Inc. 85 Ben Fairless Dr. Fairless Hills, PA 19030 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-12-19 |
| Decision Date | 2017-05-15 |
| Summary: | summary |