The following data is part of a premarket notification filed by United Orthopedic Corp. with the FDA for U2 Total Knee System.
Device ID | K051640 |
510k Number | K051640 |
Device Name: | U2 TOTAL KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | UNITED ORTHOPEDIC CORP. 57 PARK AVE. 2, SCIENCE PARK Hsinchu, TW 300 |
Contact | Gene Huang |
Correspondent | Gene Huang UNITED ORTHOPEDIC CORP. 57 PARK AVE. 2, SCIENCE PARK Hsinchu, TW 300 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-06-20 |
Decision Date | 2006-03-01 |
Summary: | summary |