The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Legion Hinge Knee System.
Device ID | K081111 |
510k Number | K081111 |
Device Name: | LEGION HINGE KNEE SYSTEM |
Classification | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer |
Applicant | SMITH & NEPHEW, INC. 1450 E BROOKS ROAD Memphis, TN 38116 |
Contact | Nicholas B Tabrizi |
Correspondent | Nicholas B Tabrizi SMITH & NEPHEW, INC. 1450 E BROOKS ROAD Memphis, TN 38116 |
Product Code | KRO |
CFR Regulation Number | 888.3510 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-04-18 |
Decision Date | 2008-07-23 |
Summary: | summary |