The following data is part of a premarket notification filed by Osstem Implant Co.,ltd with the FDA for Ms System (denture).
| Device ID | K072959 |
| 510k Number | K072959 |
| Device Name: | MS SYSTEM (DENTURE) |
| Classification | Implant, Endosseous, Root-form |
| Applicant | OSSTEM IMPLANT CO.,LTD ONE BEN FAIRLESS DR. Fairless Hills, PA 19030 |
| Contact | Min Joo Kim |
| Correspondent | Min Joo Kim OSSTEM IMPLANT CO.,LTD ONE 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 | 2007-10-19 |
| Decision Date | 2008-02-04 |
| Summary: | summary |