FDA 510(k) Applications Submitted by Natalie Williams
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K162775 |
10/03/2016 |
Legion Cone System |
Smith & Nephew, Inc. |
| K100481 |
02/18/2010 |
SMITH & NEPHEW MDF MODULAR SLEEVE |
SMITH & NEPHEW, INC. |
| K111025 |
04/13/2011 |
TRIGEN LOW PROFILE BONE SCREW |
SMITH & NEPHEW, INC. |
| K121627 |
06/04/2012 |
SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM |
SMITH & NEPHEW, INC. |
| K123012 |
09/28/2012 |
SMITH & NEPHEW SMF HIP STEM |
SMITH & NEPHEW, INC. |
| K113039 |
10/12/2011 |
SMITH & NEPHEW RADIOPAQUE TRIAL NECKS |
SMITH & NEPHEW, INC. |
| K103256 |
11/03/2010 |
SMITH & NEPHEW SMF HIP STEM |
SMITH & NEPHEW, INC. |
| K113789 |
12/22/2011 |
MODULAR PROXIMALLY FLUTED HIP STEM |
SMITH & NEPHEW, INC. |
| K151902 |
07/10/2015 |
REDAPT┐ Revision Femoral System |
SMITH & NEPHEW, INC. |
| K162641 |
09/22/2016 |
Smith & Nephew, Inc. R3Ö Constrained Liner |
Smith & Nephew, Inc. |
|
|
