The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Modified Bencox Hip System.
Device ID | K150007 |
510k Number | K150007 |
Device Name: | Modified Bencox Hip System |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
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, KR 137-040 |
Product Code | LPH |
Subsequent Product Code | KWY |
Subsequent Product Code | LZO |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-02 |
Decision Date | 2015-05-04 |
Summary: | summary |