The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Eaum Total Knee System.
| Device ID | K110404 |
| 510k Number | K110404 |
| Device Name: | EAUM TOTAL KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | CORENTEC CO., LTD 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
| Contact | Kevin A Thomas |
| Correspondent | Kevin A Thomas CORENTEC CO., LTD 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-02-14 |
| Decision Date | 2012-02-16 |
| Summary: | summary |