The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Femoral Heads.
| Device ID | K024340 |
| 510k Number | K024340 |
| Device Name: | SMITH & NEPHEW FEMORAL HEADS |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| 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 | JDI |
| Subsequent Product Code | LPH |
| Subsequent Product Code | LZO |
| CFR Regulation Number | 888.3350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-12-27 |
| Decision Date | 2003-02-26 |
| Summary: | summary |