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 |