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 |