The following data is part of a premarket notification filed by Osstem Implant Co., Ltd. with the FDA for Osstem Implant System.
Device ID | K161604 |
510k Number | K161604 |
Device Name: | OSSTEM Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | OSSTEM IMPLANT CO., LTD. 66-16, BANSONG-RO 513BEON-GIL, HAEUNDAE-GU Busan, KR 612-070 |
Contact | Hee Kwon |
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 | 2016-06-10 |
Decision Date | 2016-10-17 |