The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Lospa Modular Knee System.
Device ID | K160157 |
510k Number | K160157 |
Device Name: | LOSPA Modular Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
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 | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-01-22 |
Decision Date | 2016-12-01 |