The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Lospa Is Acp System.
Device ID | K161641 |
510k Number | K161641 |
Device Name: | LOSPA IS ACP System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | CORENTEC CO., LTD 12, YEONGSANHONG 1-GIL, IPJANG-MYEON, SEOBUK GU Cheonan-si, KR 31056 |
Contact | J.s. Daniel |
Correspondent | J.s. Daniel CORENTEC CO., LTD 8F CHUNGHO TOWER, 483, GANGNAM-DAERO, SEOCHO GU Seoul, KR 06541 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-14 |
Decision Date | 2017-01-05 |
Summary: | summary |