The following data is part of a premarket notification filed by Megagen Implant Co., Ltd with the FDA for Xpeed Anyridge Internal Implant Sysyem.
| Device ID | K140091 |
| 510k Number | K140091 |
| Device Name: | XPEED ANYRIDGE INTERNAL IMPLANT SYSYEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | MEGAGEN IMPLANT CO., LTD 325 N PUENTE ST. UNIT B Brea, CA 92821 |
| Contact | Susan Park |
| Correspondent | Susan Park MEGAGEN IMPLANT CO., LTD 325 N PUENTE ST. UNIT B Brea, CA 92821 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-01-14 |
| Decision Date | 2014-12-12 |
| Summary: | summary |