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 |