The following data is part of a premarket notification filed by Cowellmedi Co., Ltd with the FDA for Inno Sla Submerged Implant System.
Device ID | K132242 |
510k Number | K132242 |
Device Name: | INNO SLA SUBMERGED IMPLANT SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | COWELLMEDI CO., LTD 325 N. PUENTE ST UNIT B Brea, CA 92821 |
Contact | Susan Park |
Correspondent | Susan Park COWELLMEDI 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 | 2013-07-18 |
Decision Date | 2013-12-06 |
Summary: | summary |