The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Redapt¿ Revision Femoral System.
| Device ID | K151902 |
| 510k Number | K151902 |
| Device Name: | REDAPT¿ Revision Femoral System |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
| Applicant | SMITH & NEPHEW, INC. 7135 GOODLETT FARMS PARKWAY Cordova, TN 38016 |
| Contact | Natalie P. Williams |
| Correspondent | Natalie P Williams SMITH & NEPHEW, INC. 7135 GOODLETT FARMS PARKWAY Cordova, TN 38016 |
| Product Code | LZO |
| CFR Regulation Number | 888.3353 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-10 |
| Decision Date | 2015-09-03 |
| Summary: | summary |