The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Redapt Revision Femoral System.
| Device ID | K121627 |
| 510k Number | K121627 |
| Device Name: | SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate |
| 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 | MEH |
| CFR Regulation Number | 888.3353 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-04 |
| Decision Date | 2012-10-15 |
| Summary: | summary |