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 |