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 |