The following data is part of a premarket notification filed by Osstem Implant Co.,ltd with the FDA for Et Prosthetic System.
Device ID | K130662 |
510k Number | K130662 |
Device Name: | ET PROSTHETIC SYSTEM |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | OSSTEM IMPLANT CO.,LTD 85 BEN FAIRLESS DR. Fairless Hills, PA 19030 |
Contact | Patrick Lim |
Correspondent | Patrick Lim OSSTEM IMPLANT CO.,LTD 85 BEN FAIRLESS DR. Fairless Hills, PA 19030 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-03-12 |
Decision Date | 2014-01-10 |
Summary: | summary |