The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Hybrid Knee Femoral.
| Device ID | K042896 |
| 510k Number | K042896 |
| Device Name: | SMITH & NEPHEW HYBRID KNEE FEMORAL |
| Classification | Prosthesis, Knee Patellofemorotibial, Partial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Contact | Kim P Kelly |
| Correspondent | Kim P Kelly SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Product Code | NPJ |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-10-20 |
| Decision Date | 2005-01-12 |
| Summary: | summary |