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 |