The following data is part of a premarket notification filed by Osstem Implant Co., Ltd.. with the FDA for Hysil Impression Materials.
Device ID | K170736 |
510k Number | K170736 |
Device Name: | HySil Impression Materials |
Classification | Material, Impression |
Applicant | Osstem Implant Co., Ltd.. 66-16, Bansong-ro 513beon-gil, Haeundae-gu Busan, KR 612-070 |
Contact | Heekwon Son |
Correspondent | David Kim HiOSSEN Inc. 85 Ben Fairless Dr. Fairless Hills, PA 19030 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-10 |
Decision Date | 2017-06-07 |
Summary: | summary |