The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Lospa Is Spinal System.
| Device ID | K151408 |
| 510k Number | K151408 |
| Device Name: | LOSPA IS Spinal System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | CORENTEC CO., LTD 12, YEONGSANHONG 1-GIL, IPJANG-MYEON Cheonan-si, KR 331-822 |
| Contact | Goon Hee Lee |
| Correspondent | J S Daniel CORENTEC CO., LTD 8F CHUNGHO TOWER, 483, GANGNAM-DAERO Seocho Gu, Seoul, KR 137-040 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-26 |
| Decision Date | 2015-10-02 |
| Summary: | summary |