The following data is part of a premarket notification filed by Hiossen Inc. with the FDA for Hiossen Implant System.
Device ID | K140934 |
510k Number | K140934 |
Device Name: | HIOSSEN IMPLANT SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | HIOSSEN INC. 85 BEN FAIRLESS DRIVE Fairless Hills, PA 19030 |
Contact | Patrick Lim |
Correspondent | Patrick Lim HIOSSEN INC. 85 BEN FAIRLESS DRIVE 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 | 2014-04-11 |
Decision Date | 2014-11-12 |
Summary: | summary |