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 |