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 |